Canonical Allele Identifier: CA2631540073

Gene: ZNF500

Linked Data

• gnomAD v4: 16-4762320-CG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.4762324del , CM000678.2:g.4762324del	GRCh38
NC_000016.9:g.4812325del , CM000678.1:g.4812325del	GRCh37
NC_000016.8:g.4752326del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000219478.11:c.613del MANE Select	ENSP00000219478.5:p.Arg205GlyfsTer20
ENST00000219478.10:c.613del	ENSP00000219478.5:p.Arg205GlyfsTer20
ENST00000545009.1:c.613del	ENSP00000445714.1:p.Arg205GlyfsTer20
ENST00000589422.1:c.*141del	ENSP00000466375.1:n.*141del
NM_001303450.1:c.613del	NP_001290379.1:p.Arg205GlyfsTer20
NM_021646.2:c.613del	NP_067678.1:p.Arg205GlyfsTer20
XM_005255243.2:c.262del	XP_005255300.1:p.Arg88GlyfsTer20
XM_011522453.1:c.613del	XP_011520755.1:p.Arg205GlyfsTer20
XM_011522454.1:c.-12del	XP_011520756.1:n.-12del
NM_021646.3:c.613del	NP_067678.1:p.Arg205GlyfsTer20
XM_005255243.4:c.262del	XP_005255300.1:p.Arg88GlyfsTer20
XM_011522453.2:c.613del	XP_011520755.1:p.Arg205GlyfsTer20
XM_011522454.3:c.-12del	XP_011520756.1:n.-12del
XM_017023121.2:c.-12del	XP_016878610.1:n.-12del
NM_001303450.2:c.613del	NP_001290379.1:p.Arg205GlyfsTer20
NM_021646.4:c.613del MANE Select	NP_067678.1:p.Arg205GlyfsTer20