Canonical Allele Identifier: CA1590705214

Gene: PDE6A

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.149898415T= , CM000667.2:g.149898415T=	GRCh38
NC_000005.9:g.149277978T= , CM000667.1:g.149277978T=	GRCh37
NC_000005.8:g.149258171T=	NCBI36
NG_009102.1:g.51379A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000255266.10:c.1355A= MANE Select	ENSP00000255266.5:p.Asp452=
ENST00000255266.9:c.1355A=	ENSP00000255266.5:p.Asp452=
ENST00000508173.5:n.1383+960A=
ENST00000613228.1:c.1112A=	ENSP00000478060.1:p.Asp371=
ENST00000617647.4:c.1112A=	ENSP00000482774.1:p.Asp371=
NM_000440.2:c.1355A=	NP_000431.2:p.Asp452=
XM_011537648.1:c.1355A=	XP_011535950.1:p.Asp452=
XM_011537649.1:c.809A=	XP_011535951.1:p.Asp270=
XM_011537650.1:c.470A=	XP_011535952.1:p.Asp157=
XM_011537651.1:c.308A=	XP_011535953.1:p.Asp103=
XM_011537652.1:c.278A=	XP_011535954.1:p.Asp93=
XM_011537653.1:c.278A=	XP_011535955.1:p.Asp93=
XM_011537654.1:c.278A=	XP_011535956.1:p.Asp93=
XM_011537650.2:c.470A=	XP_011535952.1:p.Asp157=
XM_011537651.2:c.308A=	XP_011535953.1:p.Asp103=
XM_011537653.2:c.278A=	XP_011535955.1:p.Asp93=
XM_011537654.2:c.278A=	XP_011535956.1:p.Asp93=
XM_017009572.2:c.1112A=	XP_016865061.1:p.Asp371=
NM_000440.3:c.1355A= MANE Select	NP_000431.2:p.Asp452=