Canonical Allele Identifier: CA1152147292
Gene: PARK7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.7984861T= , CM000663.2:g.7984861T= GRCh38
NC_000001.10:g.8044921T= , CM000663.1:g.8044921T= GRCh37
NC_000001.9:g.7967508T= NCBI36
NG_008271.1:g.28208T=

Transcript Alleles

HGVS Amino-acid change
ENST00000338639.10:c.410-33T= MANE Select ENSP00000340278.5:n.410-33T=
ENST00000338639.9:c.410-33T= ENSP00000340278.5:n.410-33T=
ENST00000377488.5:c.410-33T= ENSP00000366708.1:n.410-33T=
ENST00000377491.5:c.410-33T= ENSP00000366711.1:n.410-33T=
ENST00000377493.9:c.350-33T= ENSP00000466242.1:n.350-33T=
ENST00000469225.1:c.293-3T= ENSP00000466756.1:n.293-3T=
ENST00000493373.5:c.410-33T= ENSP00000465404.1:n.410-33T=
ENST00000493678.5:c.410-33T= ENSP00000418770.1:n.410-33T=
NM_001123377.1:c.410-33T= NP_001116849.1:n.410-33T=
NM_007262.4:c.410-33T= NP_009193.2:n.410-33T=
XM_005263424.2:c.410-33T= XP_005263481.1:n.410-33T=
XM_005263424.3:c.410-33T= XP_005263481.1:n.410-33T=
NM_007262.5:c.410-33T= MANE Select NP_009193.2:n.410-33T=
NM_001123377.2:c.410-33T= NP_001116849.1:n.410-33T=