Canonical Allele Identifier: CA2203508564
Gene: ZNF500 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.4762714C= , CM000678.2:g.4762714C= GRCh38
NC_000016.9:g.4812715C= , CM000678.1:g.4812715C= GRCh37
NC_000016.8:g.4752716C= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000219478.11:c.457G= MANE Select ENSP00000219478.5:p.Gly153=
ENST00000219478.10:c.457G= ENSP00000219478.5:p.Gly153=
ENST00000545009.1:c.457G= ENSP00000445714.1:p.Gly153=
ENST00000589422.1:c.415-1G= ENSP00000466375.1:n.415-1G=
NM_001303450.1:c.457G= NP_001290379.1:p.Gly153=
NM_021646.2:c.457G= NP_067678.1:p.Gly153=
XM_005255243.2:c.106G= XP_005255300.1:p.Gly36=
XM_011522453.1:c.457G= XP_011520755.1:p.Gly153=
XM_011522454.1:c.-167-1G= XP_011520756.1:n.-167-1G=
NM_021646.3:c.457G= NP_067678.1:p.Gly153=
XM_005255243.4:c.106G= XP_005255300.1:p.Gly36=
XM_011522453.2:c.457G= XP_011520755.1:p.Gly153=
XM_011522454.3:c.-167-1G= XP_011520756.1:n.-167-1G=
XM_017023121.2:c.-168G= XP_016878610.1:n.-168G=
NM_001303450.2:c.457G= NP_001290379.1:p.Gly153=
NM_021646.4:c.457G= MANE Select NP_067678.1:p.Gly153=