Canonical Allele Identifier: CA394620412

Gene: ZNF500

Linked Data

• MyVariant Identifiers: chr16:g.4812600C>A (hg19) ; chr16:g.4762599C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.4762599C>A , CM000678.2:g.4762599C>A	GRCh38
NC_000016.9:g.4812600C>A , CM000678.1:g.4812600C>A	GRCh37
NC_000016.8:g.4752601C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000219478.11:c.572G>T MANE Select	ENSP00000219478.5:p.Arg191Met
ENST00000219478.10:c.572G>T	ENSP00000219478.5:p.Arg191Met
ENST00000545009.1:c.572G>T	ENSP00000445714.1:p.Arg191Met
ENST00000589422.1:c.*100G>T	ENSP00000466375.1:n.*100G>T
NM_001303450.1:c.572G>T	NP_001290379.1:p.Arg191Met
NM_021646.2:c.572G>T	NP_067678.1:p.Arg191Met
XM_005255243.2:c.221G>T	XP_005255300.1:p.Arg74Met
XM_011522453.1:c.572G>T	XP_011520755.1:p.Arg191Met
XM_011522454.1:c.-53G>T	XP_011520756.1:n.-53G>T
NM_021646.3:c.572G>T	NP_067678.1:p.Arg191Met
XM_005255243.4:c.221G>T	XP_005255300.1:p.Arg74Met
XM_011522453.2:c.572G>T	XP_011520755.1:p.Arg191Met
XM_011522454.3:c.-53G>T	XP_011520756.1:n.-53G>T
XM_017023121.2:c.-53G>T	XP_016878610.1:n.-53G>T
NM_001303450.2:c.572G>T	NP_001290379.1:p.Arg191Met
NM_021646.4:c.572G>T MANE Select	NP_067678.1:p.Arg191Met