Canonical Allele Identifier: CA721017519
Gene: ZNF500 HGNC NCBI

Linked Data

dbSNP Id: rs1260198304

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.4762630del , CM000678.2:g.4762630del GRCh38
NC_000016.9:g.4812631del , CM000678.1:g.4812631del GRCh37
NC_000016.8:g.4752632del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000219478.11:c.545del MANE Select ENSP00000219478.5:p.Pro182GlnfsTer4
ENST00000219478.10:c.545del ENSP00000219478.5:p.Pro182GlnfsTer4
ENST00000545009.1:c.545del ENSP00000445714.1:p.Pro182GlnfsTer4
ENST00000589422.1:c.*73del ENSP00000466375.1:n.*73del
NM_001303450.1:c.545del NP_001290379.1:p.Pro182GlnfsTer4
NM_021646.2:c.545del NP_067678.1:p.Pro182GlnfsTer4
XM_005255243.2:c.194del XP_005255300.1:p.Pro65GlnfsTer4
XM_011522453.1:c.545del XP_011520755.1:p.Pro182GlnfsTer4
XM_011522454.1:c.-80del XP_011520756.1:n.-80del
NM_021646.3:c.545del NP_067678.1:p.Pro182GlnfsTer4
XM_005255243.4:c.194del XP_005255300.1:p.Pro65GlnfsTer4
XM_011522453.2:c.545del XP_011520755.1:p.Pro182GlnfsTer4
XM_011522454.3:c.-80del XP_011520756.1:n.-80del
XM_017023121.2:c.-80del XP_016878610.1:n.-80del
NM_001303450.2:c.545del NP_001290379.1:p.Pro182GlnfsTer4
NM_021646.4:c.545del MANE Select NP_067678.1:p.Pro182GlnfsTer4