Canonical Allele Identifier: CA1152147924
Gene: PARK7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.7985186T= , CM000663.2:g.7985186T= GRCh38
NC_000001.10:g.8045246T= , CM000663.1:g.8045246T= GRCh37
NC_000001.9:g.7967833T= NCBI36
NG_008271.1:g.28533T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000338639.10:c.*132T= MANE Select ENSP00000340278.5:n.*132T=
ENST00000338639.9:c.*132T= ENSP00000340278.5:n.*132T=
ENST00000377491.5:c.*132T= ENSP00000366711.1:n.*132T=
ENST00000377493.9:c.*132T= ENSP00000466242.1:n.*132T=
ENST00000469225.1:c.615T= ENSP00000466756.1:n.615T=
ENST00000493678.5:c.*132T= ENSP00000418770.1:n.*132T=
NM_001123377.1:c.*132T= NP_001116849.1:n.*132T=
NM_007262.4:c.*132T= NP_009193.2:n.*132T=
XM_005263424.2:c.*132T= XP_005263481.1:n.*132T=
XM_005263424.3:c.*132T= XP_005263481.1:n.*132T=
NM_007262.5:c.*132T= MANE Select NP_009193.2:n.*132T=
NM_001123377.2:c.*132T= NP_001116849.1:n.*132T=