Canonical Allele Identifier: CA17284314

Gene: PARK7

Linked Data

• dbSNP Id: rs902203822
• gnomAD v4: 1-7965257-T-A
• MyVariant Identifiers: chr1:g.8025317T>A (hg19) ; chr1:g.7965257T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.7965257T>A , CM000663.2:g.7965257T>A	GRCh38
NC_000001.10:g.8025317T>A , CM000663.1:g.8025317T>A	GRCh37
NC_000001.9:g.7947904T>A	NCBI36
NG_008271.1:g.8604T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000338639.10:c.91-67T>A MANE Select	ENSP00000340278.5:n.91-67T>A
ENST00000338639.9:c.91-67T>A	ENSP00000340278.5:n.91-67T>A
ENST00000377488.5:c.91-67T>A	ENSP00000366708.1:n.91-67T>A
ENST00000377491.5:c.91-67T>A	ENSP00000366711.1:n.91-67T>A
ENST00000377493.9:c.91-67T>A	ENSP00000466242.1:n.91-67T>A
ENST00000460192.5:n.187-67T>A
ENST00000465354.5:n.160-67T>A
ENST00000493373.5:c.91-67T>A	ENSP00000465404.1:n.91-67T>A
ENST00000493678.5:c.91-67T>A	ENSP00000418770.1:n.91-67T>A
ENST00000497113.1:n.110-67T>A
NM_001123377.1:c.91-67T>A	NP_001116849.1:n.91-67T>A
NM_007262.4:c.91-67T>A	NP_009193.2:n.91-67T>A
XM_005263424.2:c.91-67T>A	XP_005263481.1:n.91-67T>A
XM_005263424.3:c.91-67T>A	XP_005263481.1:n.91-67T>A
NM_007262.5:c.91-67T>A MANE Select	NP_009193.2:n.91-67T>A
NM_001123377.2:c.91-67T>A	NP_001116849.1:n.91-67T>A