Canonical Allele Identifier: CA1152147906
Gene: PARK7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.7985171_7985174delinsACTT , CM000663.2:g.7985171_7985174delinsACTT GRCh38
NC_000001.10:g.8045231_8045234delinsACTT , CM000663.1:g.8045231_8045234delinsACTT GRCh37
NC_000001.9:g.7967818_7967821delinsACTT NCBI36
NG_008271.1:g.28518_28521delinsACTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000338639.10:c.*117_*120delinsACTT MANE Select ENSP00000340278.5:n.*117_*120delinsACTT
ENST00000338639.9:c.*117_*120delinsACTT ENSP00000340278.5:n.*117_*120delinsACTT
ENST00000377491.5:c.*117_*120delinsACTT ENSP00000366711.1:n.*117_*120delinsACTT
ENST00000377493.9:c.*117_*120delinsACTT ENSP00000466242.1:n.*117_*120delinsACTT
ENST00000469225.1:c.600_603delinsACTT ENSP00000466756.1:n.600_603delinsACTT
ENST00000493678.5:c.*117_*120delinsACTT ENSP00000418770.1:n.*117_*120delinsACTT
NM_001123377.1:c.*117_*120delinsACTT NP_001116849.1:n.*117_*120delinsACTT
NM_007262.4:c.*117_*120delinsACTT NP_009193.2:n.*117_*120delinsACTT
XM_005263424.2:c.*117_*120delinsACTT XP_005263481.1:n.*117_*120delinsACTT
XM_005263424.3:c.*117_*120delinsACTT XP_005263481.1:n.*117_*120delinsACTT
NM_007262.5:c.*117_*120delinsACTT MANE Select NP_009193.2:n.*117_*120delinsACTT
NM_001123377.2:c.*117_*120delinsACTT NP_001116849.1:n.*117_*120delinsACTT