Canonical Allele Identifier: CA2203508657

Gene: ZNF500

Linked Data

• dbSNP Id: rs2082222197

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.4762865_4762866insCG , CM000678.2:g.4762865_4762866insCG	GRCh38
NC_000016.9:g.4812866_4812867insCG , CM000678.1:g.4812866_4812867insCG	GRCh37
NC_000016.8:g.4752867_4752868insCG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000219478.11:c.415-110_415-109insCG MANE Select	ENSP00000219478.5:n.415-110_415-109insCG
ENST00000219478.10:c.415-110_415-109insCG	ENSP00000219478.5:n.415-110_415-109insCG
ENST00000545009.1:c.415-110_415-109insCG	ENSP00000445714.1:n.415-110_415-109insCG
ENST00000589422.1:c.415-153_415-152insCG	ENSP00000466375.1:n.415-153_415-152insCG
NM_001303450.1:c.415-110_415-109insCG	NP_001290379.1:n.415-110_415-109insCG
NM_021646.2:c.415-110_415-109insCG	NP_067678.1:n.415-110_415-109insCG
XM_005255243.2:c.64-110_64-109insCG	XP_005255300.1:n.64-110_64-109insCG
XM_011522453.1:c.415-110_415-109insCG	XP_011520755.1:n.415-110_415-109insCG
XM_011522454.1:c.-167-153_-167-152insCG	XP_011520756.1:n.-167-153_-167-152insCG
NM_021646.3:c.415-110_415-109insCG	NP_067678.1:n.415-110_415-109insCG
XM_005255243.4:c.64-110_64-109insCG	XP_005255300.1:n.64-110_64-109insCG
XM_011522453.2:c.415-110_415-109insCG	XP_011520755.1:n.415-110_415-109insCG
XM_011522454.3:c.-167-153_-167-152insCG	XP_011520756.1:n.-167-153_-167-152insCG
XM_017023121.2:c.-210-110_-210-109insCG	XP_016878610.1:n.-210-110_-210-109insCG
NM_001303450.2:c.415-110_415-109insCG	NP_001290379.1:n.415-110_415-109insCG
NM_021646.4:c.415-110_415-109insCG MANE Select	NP_067678.1:n.415-110_415-109insCG