Canonical Allele Identifier: CA2203508310

Gene: ZNF500

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.4762274G= , CM000678.2:g.4762274G=	GRCh38
NC_000016.9:g.4812275G= , CM000678.1:g.4812275G=	GRCh37
NC_000016.8:g.4752276G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000219478.11:c.660C= MANE Select	ENSP00000219478.5:p.Ser220=
ENST00000219478.10:c.660C=	ENSP00000219478.5:p.Ser220=
ENST00000545009.1:c.660C=	ENSP00000445714.1:p.Ser220=
ENST00000589422.1:c.*188C=	ENSP00000466375.1:n.*188C=
NM_001303450.1:c.660C=	NP_001290379.1:p.Ser220=
NM_021646.2:c.660C=	NP_067678.1:p.Ser220=
XM_005255243.2:c.309C=	XP_005255300.1:p.Ser103=
XM_011522453.1:c.660C=	XP_011520755.1:p.Ser220=
XM_011522454.1:c.36C=	XP_011520756.1:p.Ser12=
NM_021646.3:c.660C=	NP_067678.1:p.Ser220=
XM_005255243.4:c.309C=	XP_005255300.1:p.Ser103=
XM_011522453.2:c.660C=	XP_011520755.1:p.Ser220=
XM_011522454.3:c.36C=	XP_011520756.1:p.Ser12=
XM_017023121.2:c.36C=	XP_016878610.1:p.Ser12=
NM_001303450.2:c.660C=	NP_001290379.1:p.Ser220=
NM_021646.4:c.660C= MANE Select	NP_067678.1:p.Ser220=