Canonical Allele Identifier: CA394620955

Gene: ZNF500

Linked Data

• MyVariant Identifiers: chr16:g.4812684G>T (hg19) ; chr16:g.4762683G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.4762683G>T , CM000678.2:g.4762683G>T	GRCh38
NC_000016.9:g.4812684G>T , CM000678.1:g.4812684G>T	GRCh37
NC_000016.8:g.4752685G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000219478.11:c.488C>A MANE Select	ENSP00000219478.5:p.Ala163Asp
ENST00000219478.10:c.488C>A	ENSP00000219478.5:p.Ala163Asp
ENST00000545009.1:c.488C>A	ENSP00000445714.1:p.Ala163Asp
ENST00000589422.1:c.*16C>A	ENSP00000466375.1:n.*16C>A
NM_001303450.1:c.488C>A	NP_001290379.1:p.Ala163Asp
NM_021646.2:c.488C>A	NP_067678.1:p.Ala163Asp
XM_005255243.2:c.137C>A	XP_005255300.1:p.Ala46Asp
XM_011522453.1:c.488C>A	XP_011520755.1:p.Ala163Asp
XM_011522454.1:c.-137C>A	XP_011520756.1:n.-137C>A
NM_021646.3:c.488C>A	NP_067678.1:p.Ala163Asp
XM_005255243.4:c.137C>A	XP_005255300.1:p.Ala46Asp
XM_011522453.2:c.488C>A	XP_011520755.1:p.Ala163Asp
XM_011522454.3:c.-137C>A	XP_011520756.1:n.-137C>A
XM_017023121.2:c.-137C>A	XP_016878610.1:n.-137C>A
NM_001303450.2:c.488C>A	NP_001290379.1:p.Ala163Asp
NM_021646.4:c.488C>A MANE Select	NP_067678.1:p.Ala163Asp