Canonical Allele Identifier: CA2631540404

Gene: ZNF500

Linked Data

• gnomAD v4: 16-4762574-TCTCTCTGGCCACAACAGCGGGCCC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.4762579_4762602del , CM000678.2:g.4762579_4762602del	GRCh38
NC_000016.9:g.4812580_4812603del , CM000678.1:g.4812580_4812603del	GRCh37
NC_000016.8:g.4752581_4752604del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000219478.11:c.573_596del MANE Select	ENSP00000219478.5:p.Gly192_Arg199del
ENST00000219478.10:c.573_596del	ENSP00000219478.5:p.Gly192_Arg199del
ENST00000545009.1:c.573_596del	ENSP00000445714.1:p.Gly192_Arg199del
ENST00000589422.1:c.*101_*124del	ENSP00000466375.1:n.*101_*124del
NM_001303450.1:c.573_596del	NP_001290379.1:p.Gly192_Arg199del
NM_021646.2:c.573_596del	NP_067678.1:p.Gly192_Arg199del
XM_005255243.2:c.222_245del	XP_005255300.1:p.Gly75_Arg82del
XM_011522453.1:c.573_596del	XP_011520755.1:p.Gly192_Arg199del
XM_011522454.1:c.-52_-29del	XP_011520756.1:n.-52_-29del
NM_021646.3:c.573_596del	NP_067678.1:p.Gly192_Arg199del
XM_005255243.4:c.222_245del	XP_005255300.1:p.Gly75_Arg82del
XM_011522453.2:c.573_596del	XP_011520755.1:p.Gly192_Arg199del
XM_011522454.3:c.-52_-29del	XP_011520756.1:n.-52_-29del
XM_017023121.2:c.-52_-29del	XP_016878610.1:n.-52_-29del
NM_001303450.2:c.573_596del	NP_001290379.1:p.Gly192_Arg199del
NM_021646.4:c.573_596del MANE Select	NP_067678.1:p.Gly192_Arg199del