Canonical Allele Identifier: CA721017580

Gene: ZNF500

Linked Data

• dbSNP Id: rs1400816265
• MyVariant Identifiers: chr16:g.4812669del (hg19) ; chr16:g.4762668del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.4762668del , CM000678.2:g.4762668del	GRCh38
NC_000016.9:g.4812669del , CM000678.1:g.4812669del	GRCh37
NC_000016.8:g.4752670del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000219478.11:c.503del MANE Select	ENSP00000219478.5:p.Leu168ArgfsTer18
ENST00000219478.10:c.503del	ENSP00000219478.5:p.Leu168ArgfsTer18
ENST00000545009.1:c.503del	ENSP00000445714.1:p.Leu168ArgfsTer18
ENST00000589422.1:c.*31del	ENSP00000466375.1:n.*31del
NM_001303450.1:c.503del	NP_001290379.1:p.Leu168ArgfsTer18
NM_021646.2:c.503del	NP_067678.1:p.Leu168ArgfsTer18
XM_005255243.2:c.152del	XP_005255300.1:p.Leu51ArgfsTer18
XM_011522453.1:c.503del	XP_011520755.1:p.Leu168ArgfsTer18
XM_011522454.1:c.-122del	XP_011520756.1:n.-122del
NM_021646.3:c.503del	NP_067678.1:p.Leu168ArgfsTer18
XM_005255243.4:c.152del	XP_005255300.1:p.Leu51ArgfsTer18
XM_011522453.2:c.503del	XP_011520755.1:p.Leu168ArgfsTer18
XM_011522454.3:c.-122del	XP_011520756.1:n.-122del
XM_017023121.2:c.-122del	XP_016878610.1:n.-122del
NM_001303450.2:c.503del	NP_001290379.1:p.Leu168ArgfsTer18
NM_021646.4:c.503del MANE Select	NP_067678.1:p.Leu168ArgfsTer18