Canonical Allele Identifier: CA1273416703

Gene: CNGA3

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.98389757G= , CM000664.2:g.98389757G=	GRCh38
NC_000002.11:g.99006220G= , CM000664.1:g.99006220G=	GRCh37
NC_000002.10:g.98372652G=	NCBI36
NG_009097.1:g.48603G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000272602.7:c.549G= MANE Select	ENSP00000272602.2:p.Trp183=
ENST00000272602.6:c.549G=	ENSP00000272602.2:p.Trp183=
ENST00000393503.2:n.554G=
ENST00000393504.5:c.549G=	ENSP00000377140.1:p.Trp183=
ENST00000409937.1:c.561G=	ENSP00000386761.1:p.Trp187=
ENST00000436404.6:c.495G=	ENSP00000410070.2:p.Trp165=
NM_001079878.1:c.495G=	NP_001073347.1:p.Trp165=
NM_001298.2:c.549G=	NP_001289.1:p.Trp183=
XM_006712243.2:c.660G=	XP_006712306.1:p.Trp220=
XM_011510554.1:c.714G=	XP_011508856.1:p.Trp238=
XM_011510554.2:c.714G=	XP_011508856.1:p.Trp238=
NM_001079878.2:c.495G=	NP_001073347.1:p.Trp165=
NM_001298.3:c.549G= MANE Select	NP_001289.1:p.Trp183=