Canonical Allele Identifier: CA1273419662

Gene: CNGA3

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.98395859G= , CM000664.2:g.98395859G=	GRCh38
NC_000002.11:g.99012322G= , CM000664.1:g.99012322G=	GRCh37
NC_000002.10:g.98378754G=	NCBI36
NG_009097.1:g.54705G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272602.7:c.689G= MANE Select	ENSP00000272602.2:p.Gly230=
ENST00000272602.6:c.689G=	ENSP00000272602.2:p.Gly230=
ENST00000393504.5:c.689G=	ENSP00000377140.1:p.Gly230=
ENST00000409937.1:c.701G=	ENSP00000386761.1:p.Gly234=
ENST00000436404.6:c.635G=	ENSP00000410070.2:p.Gly212=
NM_001079878.1:c.635G=	NP_001073347.1:p.Gly212=
NM_001298.2:c.689G=	NP_001289.1:p.Gly230=
XM_006712243.2:c.800G=	XP_006712306.1:p.Gly267=
XM_011510554.1:c.854G=	XP_011508856.1:p.Gly285=
XM_011510554.2:c.854G=	XP_011508856.1:p.Gly285=
NM_001079878.2:c.635G=	NP_001073347.1:p.Gly212=
NM_001298.3:c.689G= MANE Select	NP_001289.1:p.Gly230=