Canonical Allele Identifier: CA2203508322

Gene: ZNF500

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.4762295C= , CM000678.2:g.4762295C=	GRCh38
NC_000016.9:g.4812296C= , CM000678.1:g.4812296C=	GRCh37
NC_000016.8:g.4752297C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000219478.11:c.639G= MANE Select	ENSP00000219478.5:p.Ser213=
ENST00000219478.10:c.639G=	ENSP00000219478.5:p.Ser213=
ENST00000545009.1:c.639G=	ENSP00000445714.1:p.Ser213=
ENST00000589422.1:c.*167G=	ENSP00000466375.1:n.*167G=
NM_001303450.1:c.639G=	NP_001290379.1:p.Ser213=
NM_021646.2:c.639G=	NP_067678.1:p.Ser213=
XM_005255243.2:c.288G=	XP_005255300.1:p.Ser96=
XM_011522453.1:c.639G=	XP_011520755.1:p.Ser213=
XM_011522454.1:c.15G=	XP_011520756.1:p.Ser5=
NM_021646.3:c.639G=	NP_067678.1:p.Ser213=
XM_005255243.4:c.288G=	XP_005255300.1:p.Ser96=
XM_011522453.2:c.639G=	XP_011520755.1:p.Ser213=
XM_011522454.3:c.15G=	XP_011520756.1:p.Ser5=
XM_017023121.2:c.15G=	XP_016878610.1:p.Ser5=
NM_001303450.2:c.639G=	NP_001290379.1:p.Ser213=
NM_021646.4:c.639G= MANE Select	NP_067678.1:p.Ser213=