Canonical Allele Identifier: CA1152148012
Gene: PARK7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.7985281T= , CM000663.2:g.7985281T= GRCh38
NC_000001.10:g.8045341T= , CM000663.1:g.8045341T= GRCh37
NC_000001.9:g.7967928T= NCBI36
NG_008271.1:g.28628T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000338639.10:c.*227T= MANE Select ENSP00000340278.5:n.*227T=
ENST00000377493.9:c.*227T= ENSP00000466242.1:n.*227T=
ENST00000469225.1:c.710T= ENSP00000466756.1:n.710T=
ENST00000493678.5:c.*227T= ENSP00000418770.1:n.*227T=
NM_001123377.1:c.*227T= NP_001116849.1:n.*227T=
NM_007262.4:c.*227T= NP_009193.2:n.*227T=
XM_005263424.2:c.*227T= XP_005263481.1:n.*227T=
XM_005263424.3:c.*227T= XP_005263481.1:n.*227T=
NM_007262.5:c.*227T= MANE Select NP_009193.2:n.*227T=
NM_001123377.2:c.*227T= NP_001116849.1:n.*227T=