Canonical Allele Identifier: CA361695126

Gene: PDE6A

Linked Data

• gnomAD v4: 5-149895228-C-G
• MyVariant Identifiers: chr5:g.149274791C>G (hg19) ; chr5:g.149895228C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.149895228C>G , CM000667.2:g.149895228C>G	GRCh38
NC_000005.9:g.149274791C>G , CM000667.1:g.149274791C>G	GRCh37
NC_000005.8:g.149254984C>G	NCBI36
NG_009102.1:g.54566G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255266.10:c.1683G>C MANE Select	ENSP00000255266.5:p.Trp561Cys
ENST00000255266.9:c.1683G>C	ENSP00000255266.5:p.Trp561Cys
ENST00000508173.5:n.1867G>C
ENST00000613228.1:c.1440G>C	ENSP00000478060.1:p.Trp480Cys
ENST00000617647.4:c.1440G>C	ENSP00000482774.1:p.Trp480Cys
NM_000440.2:c.1683G>C	NP_000431.2:p.Trp561Cys
XM_011537648.1:c.1683G>C	XP_011535950.1:p.Trp561Cys
XM_011537649.1:c.1137G>C	XP_011535951.1:p.Trp379Cys
XM_011537650.1:c.798G>C	XP_011535952.1:p.Trp266Cys
XM_011537651.1:c.636G>C	XP_011535953.1:p.Trp212Cys
XM_011537652.1:c.606G>C	XP_011535954.1:p.Trp202Cys
XM_011537653.1:c.606G>C	XP_011535955.1:p.Trp202Cys
XM_011537654.1:c.606G>C	XP_011535956.1:p.Trp202Cys
XM_011537650.2:c.798G>C	XP_011535952.1:p.Trp266Cys
XM_011537651.2:c.636G>C	XP_011535953.1:p.Trp212Cys
XM_011537653.2:c.606G>C	XP_011535955.1:p.Trp202Cys
XM_011537654.2:c.606G>C	XP_011535956.1:p.Trp202Cys
XM_017009572.2:c.1440G>C	XP_016865061.1:p.Trp480Cys
NM_000440.3:c.1683G>C MANE Select	NP_000431.2:p.Trp561Cys