Canonical Allele Identifier: CA2203508757
Gene: ZNF500 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.4763033_4763034delinsTG , CM000678.2:g.4763033_4763034delinsTG GRCh38
NC_000016.9:g.4813034_4813035delinsTG , CM000678.1:g.4813034_4813035delinsTG GRCh37
NC_000016.8:g.4753035_4753036delinsTG NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000219478.11:c.415-278_415-277delinsCA MANE Select ENSP00000219478.5:n.415-278_415-277delinsCA
ENST00000219478.10:c.415-278_415-277delinsCA ENSP00000219478.5:n.415-278_415-277delinsCA
ENST00000545009.1:c.415-278_415-277delinsCA ENSP00000445714.1:n.415-278_415-277delinsCA
ENST00000589422.1:c.415-321_415-320delinsCA ENSP00000466375.1:n.415-321_415-320delinsCA
NM_001303450.1:c.415-278_415-277delinsCA NP_001290379.1:n.415-278_415-277delinsCA
NM_021646.2:c.415-278_415-277delinsCA NP_067678.1:n.415-278_415-277delinsCA
XM_005255243.2:c.64-278_64-277delinsCA XP_005255300.1:n.64-278_64-277delinsCA
XM_011522453.1:c.415-278_415-277delinsCA XP_011520755.1:n.415-278_415-277delinsCA
XM_011522454.1:c.-167-321_-167-320delinsCA XP_011520756.1:n.-167-321_-167-320delinsCA
NM_021646.3:c.415-278_415-277delinsCA NP_067678.1:n.415-278_415-277delinsCA
XM_005255243.4:c.64-278_64-277delinsCA XP_005255300.1:n.64-278_64-277delinsCA
XM_011522453.2:c.415-278_415-277delinsCA XP_011520755.1:n.415-278_415-277delinsCA
XM_011522454.3:c.-167-321_-167-320delinsCA XP_011520756.1:n.-167-321_-167-320delinsCA
XM_017023121.2:c.-254_-253delinsCA XP_016878610.1:n.-254_-253delinsCA
NM_001303450.2:c.415-278_415-277delinsCA NP_001290379.1:n.415-278_415-277delinsCA
NM_021646.4:c.415-278_415-277delinsCA MANE Select NP_067678.1:n.415-278_415-277delinsCA