Canonical Allele Identifier: CA721017259

Gene: ZNF500

Linked Data

• dbSNP Id: rs1156932893
• gnomAD v4: 16-4762347-CAG-C
• MyVariant Identifiers: chr16:g.4812349_4812350del (hg19) ; chr16:g.4762348_4762349del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.4762350_4762351del , CM000678.2:g.4762350_4762351del	GRCh38
NC_000016.9:g.4812351_4812352del , CM000678.1:g.4812351_4812352del	GRCh37
NC_000016.8:g.4752352_4752353del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000219478.11:c.599-14_599-13del MANE Select	ENSP00000219478.5:n.599-14_599-13del
ENST00000219478.10:c.599-14_599-13del	ENSP00000219478.5:n.599-14_599-13del
ENST00000545009.1:c.599-14_599-13del	ENSP00000445714.1:n.599-14_599-13del
ENST00000589422.1:c.*127-14_*127-13del	ENSP00000466375.1:n.*127-14_*127-13del
NM_001303450.1:c.599-14_599-13del	NP_001290379.1:n.599-14_599-13del
NM_021646.2:c.599-14_599-13del	NP_067678.1:n.599-14_599-13del
XM_005255243.2:c.248-14_248-13del	XP_005255300.1:n.248-14_248-13del
XM_011522453.1:c.599-14_599-13del	XP_011520755.1:n.599-14_599-13del
XM_011522454.1:c.-26-14_-26-13del	XP_011520756.1:n.-26-14_-26-13del
NM_021646.3:c.599-14_599-13del	NP_067678.1:n.599-14_599-13del
XM_005255243.4:c.248-14_248-13del	XP_005255300.1:n.248-14_248-13del
XM_011522453.2:c.599-14_599-13del	XP_011520755.1:n.599-14_599-13del
XM_011522454.3:c.-26-14_-26-13del	XP_011520756.1:n.-26-14_-26-13del
XM_017023121.2:c.-26-14_-26-13del	XP_016878610.1:n.-26-14_-26-13del
NM_001303450.2:c.599-14_599-13del	NP_001290379.1:n.599-14_599-13del
NM_021646.4:c.599-14_599-13del MANE Select	NP_067678.1:n.599-14_599-13del