Canonical Allele Identifier: CA1273416646

Gene: CNGA3

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.98389662A= , CM000664.2:g.98389662A=	GRCh38
NC_000002.11:g.99006125A= , CM000664.1:g.99006125A=	GRCh37
NC_000002.10:g.98372557A=	NCBI36
NG_009097.1:g.48508A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000272602.7:c.454A= MANE Select	ENSP00000272602.2:p.Lys152=
ENST00000272602.6:c.454A=	ENSP00000272602.2:p.Lys152=
ENST00000393503.2:n.459A=
ENST00000393504.5:c.454A=	ENSP00000377140.1:p.Lys152=
ENST00000409937.1:c.466A=	ENSP00000386761.1:p.Lys156=
ENST00000436404.6:c.400A=	ENSP00000410070.2:p.Lys134=
NM_001079878.1:c.400A=	NP_001073347.1:p.Lys134=
NM_001298.2:c.454A=	NP_001289.1:p.Lys152=
XM_006712243.2:c.565A=	XP_006712306.1:p.Lys189=
XM_011510554.1:c.619A=	XP_011508856.1:p.Lys207=
XM_011510554.2:c.619A=	XP_011508856.1:p.Lys207=
NM_001079878.2:c.400A=	NP_001073347.1:p.Lys134=
NM_001298.3:c.454A= MANE Select	NP_001289.1:p.Lys152=