Canonical Allele Identifier: CA2203508517

Gene: ZNF500

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.4762625_4762626delinsTG , CM000678.2:g.4762625_4762626delinsTG	GRCh38
NC_000016.9:g.4812626_4812627delinsTG , CM000678.1:g.4812626_4812627delinsTG	GRCh37
NC_000016.8:g.4752627_4752628delinsTG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000219478.11:c.545_546delinsCA MANE Select	ENSP00000219478.5:p.Pro182=
ENST00000219478.10:c.545_546delinsCA	ENSP00000219478.5:p.Pro182=
ENST00000545009.1:c.545_546delinsCA	ENSP00000445714.1:p.Pro182=
ENST00000589422.1:c.*73_*74delinsCA	ENSP00000466375.1:n.*73_*74delinsCA
NM_001303450.1:c.545_546delinsCA	NP_001290379.1:p.Pro182=
NM_021646.2:c.545_546delinsCA	NP_067678.1:p.Pro182=
XM_005255243.2:c.194_195delinsCA	XP_005255300.1:p.Pro65=
XM_011522453.1:c.545_546delinsCA	XP_011520755.1:p.Pro182=
XM_011522454.1:c.-80_-79delinsCA	XP_011520756.1:n.-80_-79delinsCA
NM_021646.3:c.545_546delinsCA	NP_067678.1:p.Pro182=
XM_005255243.4:c.194_195delinsCA	XP_005255300.1:p.Pro65=
XM_011522453.2:c.545_546delinsCA	XP_011520755.1:p.Pro182=
XM_011522454.3:c.-80_-79delinsCA	XP_011520756.1:n.-80_-79delinsCA
XM_017023121.2:c.-80_-79delinsCA	XP_016878610.1:n.-80_-79delinsCA
NM_001303450.2:c.545_546delinsCA	NP_001290379.1:p.Pro182=
NM_021646.4:c.545_546delinsCA MANE Select	NP_067678.1:p.Pro182=