Canonical Allele Identifier: CA2203508746
Gene: ZNF500 HGNC NCBI

Linked Data

dbSNP Id: rs2082224649

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.4763025_4763036del , CM000678.2:g.4763025_4763036del GRCh38
NC_000016.9:g.4813026_4813037del , CM000678.1:g.4813026_4813037del GRCh37
NC_000016.8:g.4753027_4753038del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000219478.11:c.415-267_415-256del MANE Select ENSP00000219478.5:n.415-267_415-256del
ENST00000219478.10:c.415-267_415-256del ENSP00000219478.5:n.415-267_415-256del
ENST00000545009.1:c.415-267_415-256del ENSP00000445714.1:n.415-267_415-256del
ENST00000589422.1:c.415-310_415-299del ENSP00000466375.1:n.415-310_415-299del
NM_001303450.1:c.415-267_415-256del NP_001290379.1:n.415-267_415-256del
NM_021646.2:c.415-267_415-256del NP_067678.1:n.415-267_415-256del
XM_005255243.2:c.64-267_64-256del XP_005255300.1:n.64-267_64-256del
XM_011522453.1:c.415-267_415-256del XP_011520755.1:n.415-267_415-256del
XM_011522454.1:c.-167-310_-167-299del XP_011520756.1:n.-167-310_-167-299del
NM_021646.3:c.415-267_415-256del NP_067678.1:n.415-267_415-256del
XM_005255243.4:c.64-267_64-256del XP_005255300.1:n.64-267_64-256del
XM_011522453.2:c.415-267_415-256del XP_011520755.1:n.415-267_415-256del
XM_011522454.3:c.-167-310_-167-299del XP_011520756.1:n.-167-310_-167-299del
XM_017023121.2:c.-243_-232del XP_016878610.1:n.-243_-232del
NM_001303450.2:c.415-267_415-256del NP_001290379.1:n.415-267_415-256del
NM_021646.4:c.415-267_415-256del MANE Select NP_067678.1:n.415-267_415-256del