Canonical Allele Identifier: CA1273419698

Gene: CNGA3

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.98395956T= , CM000664.2:g.98395956T=	GRCh38
NC_000002.11:g.99012419T= , CM000664.1:g.99012419T=	GRCh37
NC_000002.10:g.98378851T=	NCBI36
NG_009097.1:g.54802T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272602.7:c.786T= MANE Select	ENSP00000272602.2:p.Ala262=
ENST00000272602.6:c.786T=	ENSP00000272602.2:p.Ala262=
ENST00000393504.5:c.786T=	ENSP00000377140.1:p.Ala262=
ENST00000409937.1:c.798T=	ENSP00000386761.1:p.Ala266=
ENST00000436404.6:c.732T=	ENSP00000410070.2:p.Ala244=
NM_001079878.1:c.732T=	NP_001073347.1:p.Ala244=
NM_001298.2:c.786T=	NP_001289.1:p.Ala262=
XM_006712243.2:c.897T=	XP_006712306.1:p.Ala299=
XM_011510554.1:c.951T=	XP_011508856.1:p.Ala317=
XM_011510554.2:c.951T=	XP_011508856.1:p.Ala317=
NM_001079878.2:c.732T=	NP_001073347.1:p.Ala244=
NM_001298.3:c.786T= MANE Select	NP_001289.1:p.Ala262=