Canonical Allele Identifier: CA2203508504

Gene: ZNF500

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.4762605G= , CM000678.2:g.4762605G=	GRCh38
NC_000016.9:g.4812606G= , CM000678.1:g.4812606G=	GRCh37
NC_000016.8:g.4752607G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000219478.11:c.566C= MANE Select	ENSP00000219478.5:p.Pro189=
ENST00000219478.10:c.566C=	ENSP00000219478.5:p.Pro189=
ENST00000545009.1:c.566C=	ENSP00000445714.1:p.Pro189=
ENST00000589422.1:c.*94C=	ENSP00000466375.1:n.*94C=
NM_001303450.1:c.566C=	NP_001290379.1:p.Pro189=
NM_021646.2:c.566C=	NP_067678.1:p.Pro189=
XM_005255243.2:c.215C=	XP_005255300.1:p.Pro72=
XM_011522453.1:c.566C=	XP_011520755.1:p.Pro189=
XM_011522454.1:c.-59C=	XP_011520756.1:n.-59C=
NM_021646.3:c.566C=	NP_067678.1:p.Pro189=
XM_005255243.4:c.215C=	XP_005255300.1:p.Pro72=
XM_011522453.2:c.566C=	XP_011520755.1:p.Pro189=
XM_011522454.3:c.-59C=	XP_011520756.1:n.-59C=
XM_017023121.2:c.-59C=	XP_016878610.1:n.-59C=
NM_001303450.2:c.566C=	NP_001290379.1:p.Pro189=
NM_021646.4:c.566C= MANE Select	NP_067678.1:p.Pro189=