Canonical Allele Identifier: CA1273419661

Gene: CNGA3

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.98395856A= , CM000664.2:g.98395856A=	GRCh38
NC_000002.11:g.99012319A= , CM000664.1:g.99012319A=	GRCh37
NC_000002.10:g.98378751A=	NCBI36
NG_009097.1:g.54702A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272602.7:c.686A= MANE Select	ENSP00000272602.2:p.Gln229=
ENST00000272602.6:c.686A=	ENSP00000272602.2:p.Gln229=
ENST00000393504.5:c.686A=	ENSP00000377140.1:p.Gln229=
ENST00000409937.1:c.698A=	ENSP00000386761.1:p.Gln233=
ENST00000436404.6:c.632A=	ENSP00000410070.2:p.Gln211=
NM_001079878.1:c.632A=	NP_001073347.1:p.Gln211=
NM_001298.2:c.686A=	NP_001289.1:p.Gln229=
XM_006712243.2:c.797A=	XP_006712306.1:p.Gln266=
XM_011510554.1:c.851A=	XP_011508856.1:p.Gln284=
XM_011510554.2:c.851A=	XP_011508856.1:p.Gln284=
NM_001079878.2:c.632A=	NP_001073347.1:p.Gln211=
NM_001298.3:c.686A= MANE Select	NP_001289.1:p.Gln229=