Canonical Allele Identifier: CA2203508734

Gene: ZNF500

Linked Data

• dbSNP Id: rs2082224354

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.4762993_4762994insA , CM000678.2:g.4762993_4762994insA	GRCh38
NC_000016.9:g.4812994_4812995insA , CM000678.1:g.4812994_4812995insA	GRCh37
NC_000016.8:g.4752995_4752996insA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000219478.11:c.415-238_415-237insT MANE Select	ENSP00000219478.5:n.415-238_415-237insT
ENST00000219478.10:c.415-238_415-237insT	ENSP00000219478.5:n.415-238_415-237insT
ENST00000545009.1:c.415-238_415-237insT	ENSP00000445714.1:n.415-238_415-237insT
ENST00000589422.1:c.415-281_415-280insT	ENSP00000466375.1:n.415-281_415-280insT
NM_001303450.1:c.415-238_415-237insT	NP_001290379.1:n.415-238_415-237insT
NM_021646.2:c.415-238_415-237insT	NP_067678.1:n.415-238_415-237insT
XM_005255243.2:c.64-238_64-237insT	XP_005255300.1:n.64-238_64-237insT
XM_011522453.1:c.415-238_415-237insT	XP_011520755.1:n.415-238_415-237insT
XM_011522454.1:c.-167-281_-167-280insT	XP_011520756.1:n.-167-281_-167-280insT
NM_021646.3:c.415-238_415-237insT	NP_067678.1:n.415-238_415-237insT
XM_005255243.4:c.64-238_64-237insT	XP_005255300.1:n.64-238_64-237insT
XM_011522453.2:c.415-238_415-237insT	XP_011520755.1:n.415-238_415-237insT
XM_011522454.3:c.-167-281_-167-280insT	XP_011520756.1:n.-167-281_-167-280insT
XM_017023121.2:c.-214_-213insT	XP_016878610.1:n.-214_-213insT
NM_001303450.2:c.415-238_415-237insT	NP_001290379.1:n.415-238_415-237insT
NM_021646.4:c.415-238_415-237insT MANE Select	NP_067678.1:n.415-238_415-237insT