Canonical Allele Identifier: CA361696145

Gene: PDE6A

Linked Data

• MyVariant Identifiers: chr5:g.149277974T>C (hg19) ; chr5:g.149898411T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.149898411T>C , CM000667.2:g.149898411T>C	GRCh38
NC_000005.9:g.149277974T>C , CM000667.1:g.149277974T>C	GRCh37
NC_000005.8:g.149258167T>C	NCBI36
NG_009102.1:g.51383A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000255266.10:c.1359A>G MANE Select	ENSP00000255266.5:p.Ile453Met
ENST00000255266.9:c.1359A>G	ENSP00000255266.5:p.Ile453Met
ENST00000508173.5:n.1383+964A>G
ENST00000613228.1:c.1116A>G	ENSP00000478060.1:p.Ile372Met
ENST00000617647.4:c.1116A>G	ENSP00000482774.1:p.Ile372Met
NM_000440.2:c.1359A>G	NP_000431.2:p.Ile453Met
XM_011537648.1:c.1359A>G	XP_011535950.1:p.Ile453Met
XM_011537649.1:c.813A>G	XP_011535951.1:p.Ile271Met
XM_011537650.1:c.474A>G	XP_011535952.1:p.Ile158Met
XM_011537651.1:c.312A>G	XP_011535953.1:p.Ile104Met
XM_011537652.1:c.282A>G	XP_011535954.1:p.Ile94Met
XM_011537653.1:c.282A>G	XP_011535955.1:p.Ile94Met
XM_011537654.1:c.282A>G	XP_011535956.1:p.Ile94Met
XM_011537650.2:c.474A>G	XP_011535952.1:p.Ile158Met
XM_011537651.2:c.312A>G	XP_011535953.1:p.Ile104Met
XM_011537653.2:c.282A>G	XP_011535955.1:p.Ile94Met
XM_011537654.2:c.282A>G	XP_011535956.1:p.Ile94Met
XM_017009572.2:c.1116A>G	XP_016865061.1:p.Ile372Met
NM_000440.3:c.1359A>G MANE Select	NP_000431.2:p.Ile453Met