Canonical Allele Identifier: CA338167075

Gene: PARK7

Linked Data

• dbSNP Id: rs368420490
• gnomAD v3: 1-7984932-G-T
• gnomAD v4: 1-7984932-G-T
• MyVariant Identifiers: chr1:g.8044992G>T (hg19) ; chr1:g.7984932G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.7984932G>T , CM000663.2:g.7984932G>T	GRCh38
NC_000001.10:g.8044992G>T , CM000663.1:g.8044992G>T	GRCh37
NC_000001.9:g.7967579G>T	NCBI36
NG_008271.1:g.28279G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338639.10:c.448G>T MANE Select	ENSP00000340278.5:p.Gly150Cys
ENST00000338639.9:c.448G>T	ENSP00000340278.5:p.Gly150Cys
ENST00000377488.5:c.448G>T	ENSP00000366708.1:p.Gly150Cys
ENST00000377491.5:c.448G>T	ENSP00000366711.1:p.Gly150Cys
ENST00000377493.9:c.388G>T	ENSP00000466242.1:p.Gly130Cys
ENST00000469225.1:c.361G>T	ENSP00000466756.1:p.Gly121Cys
ENST00000493373.5:c.448G>T	ENSP00000465404.1:p.Gly150Cys
ENST00000493678.5:c.448G>T	ENSP00000418770.1:p.Gly150Cys
NM_001123377.1:c.448G>T	NP_001116849.1:p.Gly150Cys
NM_007262.4:c.448G>T	NP_009193.2:p.Gly150Cys
XM_005263424.2:c.448G>T	XP_005263481.1:p.Gly150Cys
XM_005263424.3:c.448G>T	XP_005263481.1:p.Gly150Cys
NM_007262.5:c.448G>T MANE Select	NP_009193.2:p.Gly150Cys
NM_001123377.2:c.448G>T	NP_001116849.1:p.Gly150Cys