Canonical Allele Identifier: CA1152179218
Gene: PARK7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.7965264A= , CM000663.2:g.7965264A= GRCh38
NC_000001.10:g.8025324A= , CM000663.1:g.8025324A= GRCh37
NC_000001.9:g.7947911A= NCBI36
NG_008271.1:g.8611A=

Transcript Alleles

HGVS Amino-acid change
ENST00000338639.10:c.91-60A= MANE Select ENSP00000340278.5:n.91-60A=
ENST00000338639.9:c.91-60A= ENSP00000340278.5:n.91-60A=
ENST00000377488.5:c.91-60A= ENSP00000366708.1:n.91-60A=
ENST00000377491.5:c.91-60A= ENSP00000366711.1:n.91-60A=
ENST00000377493.9:c.91-60A= ENSP00000466242.1:n.91-60A=
ENST00000460192.5:n.187-60A=
ENST00000465354.5:n.160-60A=
ENST00000493373.5:c.91-60A= ENSP00000465404.1:n.91-60A=
ENST00000493678.5:c.91-60A= ENSP00000418770.1:n.91-60A=
ENST00000497113.1:n.110-60A=
NM_001123377.1:c.91-60A= NP_001116849.1:n.91-60A=
NM_007262.4:c.91-60A= NP_009193.2:n.91-60A=
XM_005263424.2:c.91-60A= XP_005263481.1:n.91-60A=
XM_005263424.3:c.91-60A= XP_005263481.1:n.91-60A=
NM_007262.5:c.91-60A= MANE Select NP_009193.2:n.91-60A=
NM_001123377.2:c.91-60A= NP_001116849.1:n.91-60A=