Canonical Allele Identifier: CA2203508506
Gene: ZNF500 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.4762610G= , CM000678.2:g.4762610G= GRCh38
NC_000016.9:g.4812611G= , CM000678.1:g.4812611G= GRCh37
NC_000016.8:g.4752612G= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000219478.11:c.561C= MANE Select ENSP00000219478.5:p.His187=
ENST00000219478.10:c.561C= ENSP00000219478.5:p.His187=
ENST00000545009.1:c.561C= ENSP00000445714.1:p.His187=
ENST00000589422.1:c.*89C= ENSP00000466375.1:n.*89C=
NM_001303450.1:c.561C= NP_001290379.1:p.His187=
NM_021646.2:c.561C= NP_067678.1:p.His187=
XM_005255243.2:c.210C= XP_005255300.1:p.His70=
XM_011522453.1:c.561C= XP_011520755.1:p.His187=
XM_011522454.1:c.-64C= XP_011520756.1:n.-64C=
NM_021646.3:c.561C= NP_067678.1:p.His187=
XM_005255243.4:c.210C= XP_005255300.1:p.His70=
XM_011522453.2:c.561C= XP_011520755.1:p.His187=
XM_011522454.3:c.-64C= XP_011520756.1:n.-64C=
XM_017023121.2:c.-64C= XP_016878610.1:n.-64C=
NM_001303450.2:c.561C= NP_001290379.1:p.His187=
NM_021646.4:c.561C= MANE Select NP_067678.1:p.His187=