Canonical Allele Identifier: CA1590695965

Gene: PDE6A

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.149886267C= , CM000667.2:g.149886267C=	GRCh38
NC_000005.9:g.149265830C= , CM000667.1:g.149265830C=	GRCh37
NC_000005.8:g.149246023C=	NCBI36
NG_009102.1:g.63527G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255266.10:c.1836G= MANE Select	ENSP00000255266.5:p.Met612=
ENST00000255266.9:c.1836G=	ENSP00000255266.5:p.Met612=
ENST00000508173.5:n.2020G=
ENST00000613228.1:c.1593G=	ENSP00000478060.1:p.Met531=
ENST00000617647.4:c.1593G=	ENSP00000482774.1:p.Met531=
NM_000440.2:c.1836G=	NP_000431.2:p.Met612=
XM_011537648.1:c.1836G=	XP_011535950.1:p.Met612=
XM_011537649.1:c.1290G=	XP_011535951.1:p.Met430=
XM_011537650.1:c.951G=	XP_011535952.1:p.Met317=
XM_011537651.1:c.789G=	XP_011535953.1:p.Met263=
XM_011537652.1:c.759G=	XP_011535954.1:p.Met253=
XM_011537653.1:c.759G=	XP_011535955.1:p.Met253=
XM_011537654.1:c.759G=	XP_011535956.1:p.Met253=
XM_011537650.2:c.951G=	XP_011535952.1:p.Met317=
XM_011537651.2:c.789G=	XP_011535953.1:p.Met263=
XM_011537653.2:c.759G=	XP_011535955.1:p.Met253=
XM_011537654.2:c.759G=	XP_011535956.1:p.Met253=
XM_017009572.2:c.1593G=	XP_016865061.1:p.Met531=
NM_000440.3:c.1836G= MANE Select	NP_000431.2:p.Met612=