Human (GRCh37.p13)
Description

hematopoietic SH2 domain containing [Source:HGNC Symbol;Acc:24920]

Gene Synonyms

ALX, FLJ14886, HSH2

Location

Chromosome 19: 16,244,838-16,269,386 forward strand.

GRCh37:CM000681.1

About this gene

This gene has 10 transcripts (splice variants), 183 orthologues and 4 paralogues.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeqFlags
ENST00000593154.2HSH2D-0092367300aaENSP00000464833.2
 
Protein coding
K7ERI2 K7ES08 NM_032855.2GENCODE Basic
ENST00000253680.6HSH2D-2012329352aaENSP00000253680.6
 
Protein coding
K7ES08 Q96JZ2 -GENCODE Basic
ENST00000397372.4HSH2D-2021990262aaENSP00000380528.4
 
Protein coding
H7BYQ7 -GENCODE Basic
ENST00000588246.1HSH2D-0011958300aaENSP00000468268.1
 
Protein coding
K7ERI2 K7ES08 -GENCODE Basic
ENST00000593031.1HSH2D-007585173aaENSP00000467189.1
 
Protein coding
K7EP18 -CDS 3' incomplete
ENST00000535834.1HSH2D-003982162aaENSP00000442140.1
 
Nonsense mediated decay
B4DT26 -Ensembl Canonical
ENST00000589463.1HSH2D-002247469aaENSP00000467576.1
 
Nonsense mediated decay
K7EPX4 --
ENST00000587963.1HSH2D-004150985aaENSP00000465636.1
 
Nonsense mediated decay
K7EKI5 --
ENST00000586872.1HSH2D-005136472aaENSP00000468495.1
 
Nonsense mediated decay
K7ES08 --
ENST00000591154.1HSH2D-00850740aaENSP00000468142.1
 
Nonsense mediated decay
--CDS 5' incomplete