Canonical Allele Identifier: CA2203508539

Gene: ZNF500

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.4762667_4762668delinsCA , CM000678.2:g.4762667_4762668delinsCA	GRCh38
NC_000016.9:g.4812668_4812669delinsCA , CM000678.1:g.4812668_4812669delinsCA	GRCh37
NC_000016.8:g.4752669_4752670delinsCA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000219478.11:c.503_504delinsTG MANE Select	ENSP00000219478.5:p.Leu168=
ENST00000219478.10:c.503_504delinsTG	ENSP00000219478.5:p.Leu168=
ENST00000545009.1:c.503_504delinsTG	ENSP00000445714.1:p.Leu168=
ENST00000589422.1:c.*31_*32delinsTG	ENSP00000466375.1:n.*31_*32delinsTG
NM_001303450.1:c.503_504delinsTG	NP_001290379.1:p.Leu168=
NM_021646.2:c.503_504delinsTG	NP_067678.1:p.Leu168=
XM_005255243.2:c.152_153delinsTG	XP_005255300.1:p.Leu51=
XM_011522453.1:c.503_504delinsTG	XP_011520755.1:p.Leu168=
XM_011522454.1:c.-122_-121delinsTG	XP_011520756.1:n.-122_-121delinsTG
NM_021646.3:c.503_504delinsTG	NP_067678.1:p.Leu168=
XM_005255243.4:c.152_153delinsTG	XP_005255300.1:p.Leu51=
XM_011522453.2:c.503_504delinsTG	XP_011520755.1:p.Leu168=
XM_011522454.3:c.-122_-121delinsTG	XP_011520756.1:n.-122_-121delinsTG
XM_017023121.2:c.-122_-121delinsTG	XP_016878610.1:n.-122_-121delinsTG
NM_001303450.2:c.503_504delinsTG	NP_001290379.1:p.Leu168=
NM_021646.4:c.503_504delinsTG MANE Select	NP_067678.1:p.Leu168=