Canonical Allele Identifier: CA415839162
Gene: PARK7 HGNC NCBI

Linked Data

gnomAD v4: 1-7985009-G-A
MyVariant Identifiers: chr1:g.8045069G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.7985009G>A , CM000663.2:g.7985009G>A GRCh38
NC_000001.10:g.8045069G>A , CM000663.1:g.8045069G>A GRCh37
NC_000001.9:g.7967656G>A NCBI36
NG_008271.1:g.28356G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000338639.10:c.525G>A MANE Select ENSP00000340278.5:p.Lys175=
ENST00000338639.9:c.525G>A ENSP00000340278.5:p.Lys175=
ENST00000377488.5:c.525G>A ENSP00000366708.1:p.Lys175=
ENST00000377491.5:c.525G>A ENSP00000366711.1:p.Lys175=
ENST00000377493.9:c.465G>A ENSP00000466242.1:p.Lys155=
ENST00000469225.1:c.438G>A ENSP00000466756.1:p.Lys146=
ENST00000493373.5:c.525G>A ENSP00000465404.1:p.Lys175=
ENST00000493678.5:c.525G>A ENSP00000418770.1:p.Lys175=
NM_001123377.1:c.525G>A NP_001116849.1:p.Lys175=
NM_007262.4:c.525G>A NP_009193.2:p.Lys175=
XM_005263424.2:c.525G>A XP_005263481.1:p.Lys175=
XM_005263424.3:c.525G>A XP_005263481.1:p.Lys175=
NM_007262.5:c.525G>A MANE Select NP_009193.2:p.Lys175=
NM_001123377.2:c.525G>A NP_001116849.1:p.Lys175=