Canonical Allele Identifier: CA2203508557

Gene: ZNF500

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.4762700_4762703delinsTAAG , CM000678.2:g.4762700_4762703delinsTAAG	GRCh38
NC_000016.9:g.4812701_4812704delinsTAAG , CM000678.1:g.4812701_4812704delinsTAAG	GRCh37
NC_000016.8:g.4752702_4752705delinsTAAG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000219478.11:c.468_471delinsCTTA MANE Select	ENSP00000219478.5:p.Phe156=
ENST00000219478.10:c.468_471delinsCTTA	ENSP00000219478.5:p.Phe156=
ENST00000545009.1:c.468_471delinsCTTA	ENSP00000445714.1:p.Phe156=
ENST00000589422.1:c.425_428delinsCTTA	ENSP00000466375.1:p.Ser142=
NM_001303450.1:c.468_471delinsCTTA	NP_001290379.1:p.Phe156=
NM_021646.2:c.468_471delinsCTTA	NP_067678.1:p.Phe156=
XM_005255243.2:c.117_120delinsCTTA	XP_005255300.1:p.Phe39=
XM_011522453.1:c.468_471delinsCTTA	XP_011520755.1:p.Phe156=
XM_011522454.1:c.-157_-154delinsCTTA	XP_011520756.1:n.-157_-154delinsCTTA
NM_021646.3:c.468_471delinsCTTA	NP_067678.1:p.Phe156=
XM_005255243.4:c.117_120delinsCTTA	XP_005255300.1:p.Phe39=
XM_011522453.2:c.468_471delinsCTTA	XP_011520755.1:p.Phe156=
XM_011522454.3:c.-157_-154delinsCTTA	XP_011520756.1:n.-157_-154delinsCTTA
XM_017023121.2:c.-157_-154delinsCTTA	XP_016878610.1:n.-157_-154delinsCTTA
NM_001303450.2:c.468_471delinsCTTA	NP_001290379.1:p.Phe156=
NM_021646.4:c.468_471delinsCTTA MANE Select	NP_067678.1:p.Phe156=