Canonical Allele Identifier: CA2203508503

Gene: ZNF500

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.4762604T= , CM000678.2:g.4762604T=	GRCh38
NC_000016.9:g.4812605T= , CM000678.1:g.4812605T=	GRCh37
NC_000016.8:g.4752606T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000219478.11:c.567A= MANE Select	ENSP00000219478.5:p.Pro189=
ENST00000219478.10:c.567A=	ENSP00000219478.5:p.Pro189=
ENST00000545009.1:c.567A=	ENSP00000445714.1:p.Pro189=
ENST00000589422.1:c.*95A=	ENSP00000466375.1:n.*95A=
NM_001303450.1:c.567A=	NP_001290379.1:p.Pro189=
NM_021646.2:c.567A=	NP_067678.1:p.Pro189=
XM_005255243.2:c.216A=	XP_005255300.1:p.Pro72=
XM_011522453.1:c.567A=	XP_011520755.1:p.Pro189=
XM_011522454.1:c.-58A=	XP_011520756.1:n.-58A=
NM_021646.3:c.567A=	NP_067678.1:p.Pro189=
XM_005255243.4:c.216A=	XP_005255300.1:p.Pro72=
XM_011522453.2:c.567A=	XP_011520755.1:p.Pro189=
XM_011522454.3:c.-58A=	XP_011520756.1:n.-58A=
XM_017023121.2:c.-58A=	XP_016878610.1:n.-58A=
NM_001303450.2:c.567A=	NP_001290379.1:p.Pro189=
NM_021646.4:c.567A= MANE Select	NP_067678.1:p.Pro189=