Canonical Allele Identifier: CA1152147212
Gene: PARK7 HGNC NCBI

Linked Data

dbSNP Id: rs1640783415
gnomAD v4: 1-7984750-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.7984750G>A , CM000663.2:g.7984750G>A GRCh38
NC_000001.10:g.8044810G>A , CM000663.1:g.8044810G>A GRCh37
NC_000001.9:g.7967397G>A NCBI36
NG_008271.1:g.28097G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000338639.10:c.410-144G>A MANE Select ENSP00000340278.5:n.410-144G>A
ENST00000338639.9:c.410-144G>A ENSP00000340278.5:n.410-144G>A
ENST00000377488.5:c.410-144G>A ENSP00000366708.1:n.410-144G>A
ENST00000377491.5:c.410-144G>A ENSP00000366711.1:n.410-144G>A
ENST00000377493.9:c.350-144G>A ENSP00000466242.1:n.350-144G>A
ENST00000469225.1:c.293-114G>A ENSP00000466756.1:n.293-114G>A
ENST00000493373.5:c.410-144G>A ENSP00000465404.1:n.410-144G>A
ENST00000493678.5:c.410-144G>A ENSP00000418770.1:n.410-144G>A
NM_001123377.1:c.410-144G>A NP_001116849.1:n.410-144G>A
NM_007262.4:c.410-144G>A NP_009193.2:n.410-144G>A
XM_005263424.2:c.410-144G>A XP_005263481.1:n.410-144G>A
XM_005263424.3:c.410-144G>A XP_005263481.1:n.410-144G>A
NM_007262.5:c.410-144G>A MANE Select NP_009193.2:n.410-144G>A
NM_001123377.2:c.410-144G>A NP_001116849.1:n.410-144G>A