Canonical Allele Identifier: CA2643056839
Gene: PARK7 HGNC NCBI

Linked Data

gnomAD v4: 1-7984781-GT-G

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.7984783del , CM000663.2:g.7984783del GRCh38
NC_000001.10:g.8044843del , CM000663.1:g.8044843del GRCh37
NC_000001.9:g.7967430del NCBI36
NG_008271.1:g.28130del

Transcript Alleles

HGVS Amino-acid Change
ENST00000338639.10:c.410-111del MANE Select ENSP00000340278.5:n.410-111del
ENST00000338639.9:c.410-111del ENSP00000340278.5:n.410-111del
ENST00000377488.5:c.410-111del ENSP00000366708.1:n.410-111del
ENST00000377491.5:c.410-111del ENSP00000366711.1:n.410-111del
ENST00000377493.9:c.350-111del ENSP00000466242.1:n.350-111del
ENST00000469225.1:c.293-81del ENSP00000466756.1:n.293-81del
ENST00000493373.5:c.410-111del ENSP00000465404.1:n.410-111del
ENST00000493678.5:c.410-111del ENSP00000418770.1:n.410-111del
NM_001123377.1:c.410-111del NP_001116849.1:n.410-111del
NM_007262.4:c.410-111del NP_009193.2:n.410-111del
XM_005263424.2:c.410-111del XP_005263481.1:n.410-111del
XM_005263424.3:c.410-111del XP_005263481.1:n.410-111del
NM_007262.5:c.410-111del MANE Select NP_009193.2:n.410-111del
NM_001123377.2:c.410-111del NP_001116849.1:n.410-111del