Canonical Allele Identifier: CA1273419682

Gene: CNGA3

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.98395927G= , CM000664.2:g.98395927G=	GRCh38
NC_000002.11:g.99012390G= , CM000664.1:g.99012390G=	GRCh37
NC_000002.10:g.98378822G=	NCBI36
NG_009097.1:g.54773G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000272602.7:c.757G= MANE Select	ENSP00000272602.2:p.Val253=
ENST00000272602.6:c.757G=	ENSP00000272602.2:p.Val253=
ENST00000393504.5:c.757G=	ENSP00000377140.1:p.Val253=
ENST00000409937.1:c.769G=	ENSP00000386761.1:p.Val257=
ENST00000436404.6:c.703G=	ENSP00000410070.2:p.Val235=
NM_001079878.1:c.703G=	NP_001073347.1:p.Val235=
NM_001298.2:c.757G=	NP_001289.1:p.Val253=
XM_006712243.2:c.868G=	XP_006712306.1:p.Val290=
XM_011510554.1:c.922G=	XP_011508856.1:p.Val308=
XM_011510554.2:c.922G=	XP_011508856.1:p.Val308=
NM_001079878.2:c.703G=	NP_001073347.1:p.Val235=
NM_001298.3:c.757G= MANE Select	NP_001289.1:p.Val253=