Canonical Allele Identifier: CA1590702437

Gene: PDE6A

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.149895195G= , CM000667.2:g.149895195G=	GRCh38
NC_000005.9:g.149274758G= , CM000667.1:g.149274758G=	GRCh37
NC_000005.8:g.149254951G=	NCBI36
NG_009102.1:g.54599C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255266.10:c.1716C= MANE Select	ENSP00000255266.5:p.Phe572=
ENST00000255266.9:c.1716C=	ENSP00000255266.5:p.Phe572=
ENST00000508173.5:n.1900C=
ENST00000613228.1:c.1473C=	ENSP00000478060.1:p.Phe491=
ENST00000617647.4:c.1473C=	ENSP00000482774.1:p.Phe491=
NM_000440.2:c.1716C=	NP_000431.2:p.Phe572=
XM_011537648.1:c.1716C=	XP_011535950.1:p.Phe572=
XM_011537649.1:c.1170C=	XP_011535951.1:p.Phe390=
XM_011537650.1:c.831C=	XP_011535952.1:p.Phe277=
XM_011537651.1:c.669C=	XP_011535953.1:p.Phe223=
XM_011537652.1:c.639C=	XP_011535954.1:p.Phe213=
XM_011537653.1:c.639C=	XP_011535955.1:p.Phe213=
XM_011537654.1:c.639C=	XP_011535956.1:p.Phe213=
XM_011537650.2:c.831C=	XP_011535952.1:p.Phe277=
XM_011537651.2:c.669C=	XP_011535953.1:p.Phe223=
XM_011537653.2:c.639C=	XP_011535955.1:p.Phe213=
XM_011537654.2:c.639C=	XP_011535956.1:p.Phe213=
XM_017009572.2:c.1473C=	XP_016865061.1:p.Phe491=
NM_000440.3:c.1716C= MANE Select	NP_000431.2:p.Phe572=