Canonical Allele Identifier: CA1273418699

Gene: CNGA3

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.98393775G= , CM000664.2:g.98393775G=	GRCh38
NC_000002.11:g.99010238G= , CM000664.1:g.99010238G=	GRCh37
NC_000002.10:g.98376670G=	NCBI36
NG_009097.1:g.52621G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272602.7:c.673+1805G= MANE Select	ENSP00000272602.2:n.673+1805G=
ENST00000272602.6:c.673+1805G=	ENSP00000272602.2:n.673+1805G=
ENST00000393504.5:c.673+1805G=	ENSP00000377140.1:n.673+1805G=
ENST00000409937.1:c.685+1805G=	ENSP00000386761.1:n.685+1805G=
ENST00000436404.6:c.619+1805G=	ENSP00000410070.2:n.619+1805G=
NM_001079878.1:c.619+1805G=	NP_001073347.1:n.619+1805G=
NM_001298.2:c.673+1805G=	NP_001289.1:n.673+1805G=
XM_006712243.2:c.784+1805G=	XP_006712306.1:n.784+1805G=
XM_011510554.1:c.838+1805G=	XP_011508856.1:n.838+1805G=
XM_011510554.2:c.838+1805G=	XP_011508856.1:n.838+1805G=
NM_001079878.2:c.619+1805G=	NP_001073347.1:n.619+1805G=
NM_001298.3:c.673+1805G= MANE Select	NP_001289.1:n.673+1805G=