Canonical Allele Identifier: CA1152147957
Gene: PARK7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.7985218C= , CM000663.2:g.7985218C= GRCh38
NC_000001.10:g.8045278C= , CM000663.1:g.8045278C= GRCh37
NC_000001.9:g.7967865C= NCBI36
NG_008271.1:g.28565C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000338639.10:c.*164C= MANE Select ENSP00000340278.5:n.*164C=
ENST00000338639.9:c.*164C= ENSP00000340278.5:n.*164C=
ENST00000377491.5:c.*164C= ENSP00000366711.1:n.*164C=
ENST00000377493.9:c.*164C= ENSP00000466242.1:n.*164C=
ENST00000469225.1:c.647C= ENSP00000466756.1:n.647C=
ENST00000493678.5:c.*164C= ENSP00000418770.1:n.*164C=
NM_001123377.1:c.*164C= NP_001116849.1:n.*164C=
NM_007262.4:c.*164C= NP_009193.2:n.*164C=
XM_005263424.2:c.*164C= XP_005263481.1:n.*164C=
XM_005263424.3:c.*164C= XP_005263481.1:n.*164C=
NM_007262.5:c.*164C= MANE Select NP_009193.2:n.*164C=
NM_001123377.2:c.*164C= NP_001116849.1:n.*164C=