Canonical Allele Identifier: CA394620233

Gene: ZNF500

Linked Data

• MyVariant Identifiers: chr16:g.4812283C>T (hg19) ; chr16:g.4762282C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.4762282C>T , CM000678.2:g.4762282C>T	GRCh38
NC_000016.9:g.4812283C>T , CM000678.1:g.4812283C>T	GRCh37
NC_000016.8:g.4752284C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000219478.11:c.652G>A MANE Select	ENSP00000219478.5:p.Ala218Thr
ENST00000219478.10:c.652G>A	ENSP00000219478.5:p.Ala218Thr
ENST00000545009.1:c.652G>A	ENSP00000445714.1:p.Ala218Thr
ENST00000589422.1:c.*180G>A	ENSP00000466375.1:n.*180G>A
NM_001303450.1:c.652G>A	NP_001290379.1:p.Ala218Thr
NM_021646.2:c.652G>A	NP_067678.1:p.Ala218Thr
XM_005255243.2:c.301G>A	XP_005255300.1:p.Ala101Thr
XM_011522453.1:c.652G>A	XP_011520755.1:p.Ala218Thr
XM_011522454.1:c.28G>A	XP_011520756.1:p.Ala10Thr
NM_021646.3:c.652G>A	NP_067678.1:p.Ala218Thr
XM_005255243.4:c.301G>A	XP_005255300.1:p.Ala101Thr
XM_011522453.2:c.652G>A	XP_011520755.1:p.Ala218Thr
XM_011522454.3:c.28G>A	XP_011520756.1:p.Ala10Thr
XM_017023121.2:c.28G>A	XP_016878610.1:p.Ala10Thr
NM_001303450.2:c.652G>A	NP_001290379.1:p.Ala218Thr
NM_021646.4:c.652G>A MANE Select	NP_067678.1:p.Ala218Thr