Canonical Allele Identifier: CA2631540664

Gene: ZNF500

Linked Data

• gnomAD v4: 16-4762851-CG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.4762853del , CM000678.2:g.4762853del	GRCh38
NC_000016.9:g.4812854del , CM000678.1:g.4812854del	GRCh37
NC_000016.8:g.4752855del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000219478.11:c.415-96del MANE Select	ENSP00000219478.5:n.415-96del
ENST00000219478.10:c.415-96del	ENSP00000219478.5:n.415-96del
ENST00000545009.1:c.415-96del	ENSP00000445714.1:n.415-96del
ENST00000589422.1:c.415-139del	ENSP00000466375.1:n.415-139del
NM_001303450.1:c.415-96del	NP_001290379.1:n.415-96del
NM_021646.2:c.415-96del	NP_067678.1:n.415-96del
XM_005255243.2:c.64-96del	XP_005255300.1:n.64-96del
XM_011522453.1:c.415-96del	XP_011520755.1:n.415-96del
XM_011522454.1:c.-167-139del	XP_011520756.1:n.-167-139del
NM_021646.3:c.415-96del	NP_067678.1:n.415-96del
XM_005255243.4:c.64-96del	XP_005255300.1:n.64-96del
XM_011522453.2:c.415-96del	XP_011520755.1:n.415-96del
XM_011522454.3:c.-167-139del	XP_011520756.1:n.-167-139del
XM_017023121.2:c.-210-96del	XP_016878610.1:n.-210-96del
NM_001303450.2:c.415-96del	NP_001290379.1:n.415-96del
NM_021646.4:c.415-96del MANE Select	NP_067678.1:n.415-96del