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Human (GRCh37.p13)
Description

Kallmann syndrome 1 sequence [Source:HGNC Symbol;Acc:6211]

Gene Synonyms

ADMLX, HH1, HHA, KAL, KALIG-1, KALIG1, KMS, WFDC19

Location

Chromosome X: 8,496,915-8,700,227 reverse strand.

GRCh37:CM000685.1

About this gene

This gene has 3 transcripts (splice variants) and is associated with 3 phenotypes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeqFlags
ENST00000262648.3KAL1-0016314680aaENSP00000262648.3
 
Protein coding
CCDS14130P23352 NM_000216
NP_000207
GENCODE basic
ENST00000481896.1KAL1-003797No protein-
 
Processed transcript
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ENST00000488294.1KAL1-002704No protein-
 
Processed transcript
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Gene-based displays