Canonical Allele Identifier: CA1273420094

Gene: CNGA3

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.98396848T= , CM000664.2:g.98396848T=	GRCh38
NC_000002.11:g.99013311T= , CM000664.1:g.99013311T=	GRCh37
NC_000002.10:g.98379743T=	NCBI36
NG_009097.1:g.55694T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000272602.7:c.1678T= MANE Select	ENSP00000272602.2:p.Ser560=
ENST00000272602.6:c.1678T=	ENSP00000272602.2:p.Ser560=
ENST00000393504.5:c.1678T=	ENSP00000377140.1:p.Ser560=
ENST00000409937.1:c.1690T=	ENSP00000386761.1:p.Ser564=
ENST00000436404.6:c.1624T=	ENSP00000410070.2:p.Ser542=
NM_001079878.1:c.1624T=	NP_001073347.1:p.Ser542=
NM_001298.2:c.1678T=	NP_001289.1:p.Ser560=
XM_006712243.2:c.1789T=	XP_006712306.1:p.Ser597=
XM_011510554.1:c.1843T=	XP_011508856.1:p.Ser615=
XM_011510554.2:c.1843T=	XP_011508856.1:p.Ser615=
NM_001079878.2:c.1624T=	NP_001073347.1:p.Ser542=
NM_001298.3:c.1678T= MANE Select	NP_001289.1:p.Ser560=