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Human (GRCh37.p13)
Description

calcium channel, voltage-dependent, L type, alpha 1F subunit [Source:HGNC Symbol;Acc:1393]

Gene Synonyms

AIED, CACNAF1, COD3, COD4, CORDX, CORDX3, CSNB2, CSNB2A, CSNBX2, Cav1.4, Cav1.4alpha1, JM8, JMC8, OA2

Location

Chromosome X: 49,061,523-49,089,833 reverse strand.

GRCh37:CM000685.1

View alleles of this gene on alternative sequences

About this gene

This gene has 6 transcripts (splice variants), 1 gene allele, 16 paralogues and is associated with 7 phenotypes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeqFlags
ENST00000376265.2CACNA1F-00760701977aaENSP00000365441.2
 
Protein coding
CCDS35253O60840 NM_005183.2Ensembl CanonicalGENCODE basic
ENST00000323022.5CACNA1F-00160371966aaENSP00000321618.5
 
Protein coding
CCDS59167F5CIQ9 O60840 NM_001256789.1GENCODE basic
ENST00000376251.1CACNA1F-00258131912aaENSP00000365427.1
 
Protein coding
CCDS59166O60840 NM_001256790.1GENCODE basic
ENST00000486943.1CACNA1F-005662116aaENSP00000418961.1
 
Protein coding
H7C549 -CDS 5' incomplete
ENST00000480889.1CACNA1F-006505No protein-
 
Processed transcript
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ENST00000481035.1CACNA1F-004714No protein-
 
Retained intron
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