Canonical Allele Identifier: CA447141333

Gene: PDE6A

Linked Data

• MyVariant Identifiers: chr5:g.149274746C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.149895183C>G , CM000667.2:g.149895183C>G	GRCh38
NC_000005.9:g.149274746C>G , CM000667.1:g.149274746C>G	GRCh37
NC_000005.8:g.149254939C>G	NCBI36
NG_009102.1:g.54611G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255266.10:c.1728G>C MANE Select	ENSP00000255266.5:p.Val576=
ENST00000255266.9:c.1728G>C	ENSP00000255266.5:p.Val576=
ENST00000508173.5:n.1912G>C
ENST00000613228.1:c.1485G>C	ENSP00000478060.1:p.Val495=
ENST00000617647.4:c.1485G>C	ENSP00000482774.1:p.Val495=
NM_000440.2:c.1728G>C	NP_000431.2:p.Val576=
XM_011537648.1:c.1728G>C	XP_011535950.1:p.Val576=
XM_011537649.1:c.1182G>C	XP_011535951.1:p.Val394=
XM_011537650.1:c.843G>C	XP_011535952.1:p.Val281=
XM_011537651.1:c.681G>C	XP_011535953.1:p.Val227=
XM_011537652.1:c.651G>C	XP_011535954.1:p.Val217=
XM_011537653.1:c.651G>C	XP_011535955.1:p.Val217=
XM_011537654.1:c.651G>C	XP_011535956.1:p.Val217=
XM_011537650.2:c.843G>C	XP_011535952.1:p.Val281=
XM_011537651.2:c.681G>C	XP_011535953.1:p.Val227=
XM_011537653.2:c.651G>C	XP_011535955.1:p.Val217=
XM_011537654.2:c.651G>C	XP_011535956.1:p.Val217=
XM_017009572.2:c.1485G>C	XP_016865061.1:p.Val495=
NM_000440.3:c.1728G>C MANE Select	NP_000431.2:p.Val576=