Canonical Allele Identifier: CA620507105

Gene: ZNF500

Linked Data

• dbSNP Id: rs1291112814
• gnomAD v2: 16-4812893-GC-G
• gnomAD v3: 16-4762892-GC-G
• gnomAD v4: 16-4762892-GC-G
• MyVariant Identifiers: chr16:g.4812894del (hg19) ; chr16:g.4762893del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.4762895del , CM000678.2:g.4762895del	GRCh38
NC_000016.9:g.4812896del , CM000678.1:g.4812896del	GRCh37
NC_000016.8:g.4752897del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000219478.11:c.415-137del MANE Select	ENSP00000219478.5:n.415-137del
ENST00000219478.10:c.415-137del	ENSP00000219478.5:n.415-137del
ENST00000545009.1:c.415-137del	ENSP00000445714.1:n.415-137del
ENST00000589422.1:c.415-180del	ENSP00000466375.1:n.415-180del
NM_001303450.1:c.415-137del	NP_001290379.1:n.415-137del
NM_021646.2:c.415-137del	NP_067678.1:n.415-137del
XM_005255243.2:c.64-137del	XP_005255300.1:n.64-137del
XM_011522453.1:c.415-137del	XP_011520755.1:n.415-137del
XM_011522454.1:c.-167-180del	XP_011520756.1:n.-167-180del
NM_021646.3:c.415-137del	NP_067678.1:n.415-137del
XM_005255243.4:c.64-137del	XP_005255300.1:n.64-137del
XM_011522453.2:c.415-137del	XP_011520755.1:n.415-137del
XM_011522454.3:c.-167-180del	XP_011520756.1:n.-167-180del
XM_017023121.2:c.-211+98del	XP_016878610.1:n.-211+98del
NM_001303450.2:c.415-137del	NP_001290379.1:n.415-137del
NM_021646.4:c.415-137del MANE Select	NP_067678.1:n.415-137del