Canonical Allele Identifier: CA361692712

Gene: PDE6A

Linked Data

• MyVariant Identifiers: chr5:g.149263088A>G (hg19) ; chr5:g.149883525A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.149883525A>G , CM000667.2:g.149883525A>G	GRCh38
NC_000005.9:g.149263088A>G , CM000667.1:g.149263088A>G	GRCh37
NC_000005.8:g.149243281A>G	NCBI36
NG_009102.1:g.66269T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000255266.10:c.2039T>C MANE Select	ENSP00000255266.5:p.Met680Thr
ENST00000255266.9:c.2039T>C	ENSP00000255266.5:p.Met680Thr
ENST00000508173.5:n.2223T>C
ENST00000613228.1:c.1796T>C	ENSP00000478060.1:p.Met599Thr
ENST00000617647.4:c.1796T>C	ENSP00000482774.1:p.Met599Thr
NM_000440.2:c.2039T>C	NP_000431.2:p.Met680Thr
XM_011537648.1:c.2039T>C	XP_011535950.1:p.Met680Thr
XM_011537649.1:c.1493T>C	XP_011535951.1:p.Met498Thr
XM_011537650.1:c.1154T>C	XP_011535952.1:p.Met385Thr
XM_011537651.1:c.992T>C	XP_011535953.1:p.Met331Thr
XM_011537652.1:c.962T>C	XP_011535954.1:p.Met321Thr
XM_011537653.1:c.962T>C	XP_011535955.1:p.Met321Thr
XM_011537654.1:c.962T>C	XP_011535956.1:p.Met321Thr
XM_011537650.2:c.1154T>C	XP_011535952.1:p.Met385Thr
XM_011537651.2:c.992T>C	XP_011535953.1:p.Met331Thr
XM_011537653.2:c.962T>C	XP_011535955.1:p.Met321Thr
XM_011537654.2:c.962T>C	XP_011535956.1:p.Met321Thr
XM_017009572.2:c.1796T>C	XP_016865061.1:p.Met599Thr
NM_000440.3:c.2039T>C MANE Select	NP_000431.2:p.Met680Thr