Canonical Allele Identifier: CA2805666548

Gene: ZNF500

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.4762714dup , CM000678.2:g.4762714dup	GRCh38
NC_000016.9:g.4812715dup , CM000678.1:g.4812715dup	GRCh37
NC_000016.8:g.4752716dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000219478.11:c.461dup MANE Select	ENSP00000219478.5:p.Gln155ThrfsTer?
ENST00000219478.10:c.461dup	ENSP00000219478.5:p.Gln155ThrfsTer?
ENST00000545009.1:c.461dup	ENSP00000445714.1:p.Gln155ThrfsTer?
ENST00000589422.1:c.418dup
NM_001303450.1:c.461dup	NP_001290379.1:p.Gln155ThrfsTer?
NM_021646.2:c.461dup	NP_067678.1:p.Gln155ThrfsTer?
XM_005255243.2:c.110dup	XP_005255300.1:p.Gln38ThrfsTer?
XM_011522453.1:c.461dup	XP_011520755.1:p.Gln155ThrfsTer?
XM_011522454.1:c.-164dup
NM_021646.3:c.461dup	NP_067678.1:p.Gln155ThrfsTer?
XM_005255243.4:c.110dup	XP_005255300.1:p.Gln38ThrfsTer?
XM_011522453.2:c.461dup	XP_011520755.1:p.Gln155ThrfsTer?
XM_011522454.3:c.-164dup
XM_017023121.2:c.-164dup	XP_016878610.1:n.-164dup
NM_001303450.2:c.461dup	NP_001290379.1:p.Gln155ThrfsTer?
NM_021646.4:c.461dup MANE Select	NP_067678.1:p.Gln155ThrfsTer?