Canonical Allele Identifier: CA1273419697

Gene: CNGA3

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.98395955C= , CM000664.2:g.98395955C=	GRCh38
NC_000002.11:g.99012418C= , CM000664.1:g.99012418C=	GRCh37
NC_000002.10:g.98378850C=	NCBI36
NG_009097.1:g.54801C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272602.7:c.785C= MANE Select	ENSP00000272602.2:p.Ala262=
ENST00000272602.6:c.785C=	ENSP00000272602.2:p.Ala262=
ENST00000393504.5:c.785C=	ENSP00000377140.1:p.Ala262=
ENST00000409937.1:c.797C=	ENSP00000386761.1:p.Ala266=
ENST00000436404.6:c.731C=	ENSP00000410070.2:p.Ala244=
NM_001079878.1:c.731C=	NP_001073347.1:p.Ala244=
NM_001298.2:c.785C=	NP_001289.1:p.Ala262=
XM_006712243.2:c.896C=	XP_006712306.1:p.Ala299=
XM_011510554.1:c.950C=	XP_011508856.1:p.Ala317=
XM_011510554.2:c.950C=	XP_011508856.1:p.Ala317=
NM_001079878.2:c.731C=	NP_001073347.1:p.Ala244=
NM_001298.3:c.785C= MANE Select	NP_001289.1:p.Ala262=