Canonical Allele Identifier: CA1590702581

Gene: PDE6A

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.149895246C= , CM000667.2:g.149895246C=	GRCh38
NC_000005.9:g.149274809C= , CM000667.1:g.149274809C=	GRCh37
NC_000005.8:g.149255002C=	NCBI36
NG_009102.1:g.54548G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255266.10:c.1665G= MANE Select	ENSP00000255266.5:p.Lys555=
ENST00000255266.9:c.1665G=	ENSP00000255266.5:p.Lys555=
ENST00000508173.5:n.1849G=
ENST00000613228.1:c.1422G=	ENSP00000478060.1:p.Lys474=
ENST00000617647.4:c.1422G=	ENSP00000482774.1:p.Lys474=
NM_000440.2:c.1665G=	NP_000431.2:p.Lys555=
XM_011537648.1:c.1665G=	XP_011535950.1:p.Lys555=
XM_011537649.1:c.1119G=	XP_011535951.1:p.Lys373=
XM_011537650.1:c.780G=	XP_011535952.1:p.Lys260=
XM_011537651.1:c.618G=	XP_011535953.1:p.Lys206=
XM_011537652.1:c.588G=	XP_011535954.1:p.Lys196=
XM_011537653.1:c.588G=	XP_011535955.1:p.Lys196=
XM_011537654.1:c.588G=	XP_011535956.1:p.Lys196=
XM_011537650.2:c.780G=	XP_011535952.1:p.Lys260=
XM_011537651.2:c.618G=	XP_011535953.1:p.Lys206=
XM_011537653.2:c.588G=	XP_011535955.1:p.Lys196=
XM_011537654.2:c.588G=	XP_011535956.1:p.Lys196=
XM_017009572.2:c.1422G=	XP_016865061.1:p.Lys474=
NM_000440.3:c.1665G= MANE Select	NP_000431.2:p.Lys555=