Canonical Allele Identifier: CA347833860

Gene: CNGA3

Linked Data

• COSMIC: COSM6041942
• MyVariant Identifiers: chr2:g.99013216C>T (hg19) ; chr2:g.98396753C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.98396753C>T , CM000664.2:g.98396753C>T	GRCh38
NC_000002.11:g.99013216C>T , CM000664.1:g.99013216C>T	GRCh37
NC_000002.10:g.98379648C>T	NCBI36
NG_009097.1:g.55599C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272602.7:c.1583C>T MANE Select	ENSP00000272602.2:p.Ala528Val
ENST00000272602.6:c.1583C>T	ENSP00000272602.2:p.Ala528Val
ENST00000393504.5:c.1583C>T	ENSP00000377140.1:p.Ala528Val
ENST00000409937.1:c.1595C>T	ENSP00000386761.1:p.Ala532Val
ENST00000436404.6:c.1529C>T	ENSP00000410070.2:p.Ala510Val
NM_001079878.1:c.1529C>T	NP_001073347.1:p.Ala510Val
NM_001298.2:c.1583C>T	NP_001289.1:p.Ala528Val
XM_006712243.2:c.1694C>T	XP_006712306.1:p.Ala565Val
XM_011510554.1:c.1748C>T	XP_011508856.1:p.Ala583Val
XM_011510554.2:c.1748C>T	XP_011508856.1:p.Ala583Val
NM_001079878.2:c.1529C>T	NP_001073347.1:p.Ala510Val
NM_001298.3:c.1583C>T MANE Select	NP_001289.1:p.Ala528Val