Canonical Allele Identifier: CA2203508612

Gene: ZNF500

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.4762798_4762799delinsCA , CM000678.2:g.4762798_4762799delinsCA	GRCh38
NC_000016.9:g.4812799_4812800delinsCA , CM000678.1:g.4812799_4812800delinsCA	GRCh37
NC_000016.8:g.4752800_4752801delinsCA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000219478.11:c.415-43_415-42delinsTG MANE Select	ENSP00000219478.5:n.415-43_415-42delinsTG
ENST00000219478.10:c.415-43_415-42delinsTG	ENSP00000219478.5:n.415-43_415-42delinsTG
ENST00000545009.1:c.415-43_415-42delinsTG	ENSP00000445714.1:n.415-43_415-42delinsTG
ENST00000589422.1:c.415-86_415-85delinsTG	ENSP00000466375.1:n.415-86_415-85delinsTG
NM_001303450.1:c.415-43_415-42delinsTG	NP_001290379.1:n.415-43_415-42delinsTG
NM_021646.2:c.415-43_415-42delinsTG	NP_067678.1:n.415-43_415-42delinsTG
XM_005255243.2:c.64-43_64-42delinsTG	XP_005255300.1:n.64-43_64-42delinsTG
XM_011522453.1:c.415-43_415-42delinsTG	XP_011520755.1:n.415-43_415-42delinsTG
XM_011522454.1:c.-167-86_-167-85delinsTG	XP_011520756.1:n.-167-86_-167-85delinsTG
NM_021646.3:c.415-43_415-42delinsTG	NP_067678.1:n.415-43_415-42delinsTG
XM_005255243.4:c.64-43_64-42delinsTG	XP_005255300.1:n.64-43_64-42delinsTG
XM_011522453.2:c.415-43_415-42delinsTG	XP_011520755.1:n.415-43_415-42delinsTG
XM_011522454.3:c.-167-86_-167-85delinsTG	XP_011520756.1:n.-167-86_-167-85delinsTG
XM_017023121.2:c.-210-43_-210-42delinsTG	XP_016878610.1:n.-210-43_-210-42delinsTG
NM_001303450.2:c.415-43_415-42delinsTG	NP_001290379.1:n.415-43_415-42delinsTG
NM_021646.4:c.415-43_415-42delinsTG MANE Select	NP_067678.1:n.415-43_415-42delinsTG