Canonical Allele Identifier: CA394621022

Gene: ZNF500

Linked Data

• MyVariant Identifiers: chr16:g.4812691C>A (hg19) ; chr16:g.4762690C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.4762690C>A , CM000678.2:g.4762690C>A	GRCh38
NC_000016.9:g.4812691C>A , CM000678.1:g.4812691C>A	GRCh37
NC_000016.8:g.4752692C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000219478.11:c.481G>T MANE Select	ENSP00000219478.5:p.Ala161Ser
ENST00000219478.10:c.481G>T	ENSP00000219478.5:p.Ala161Ser
ENST00000545009.1:c.481G>T	ENSP00000445714.1:p.Ala161Ser
ENST00000589422.1:c.*9G>T	ENSP00000466375.1:n.*9G>T
NM_001303450.1:c.481G>T	NP_001290379.1:p.Ala161Ser
NM_021646.2:c.481G>T	NP_067678.1:p.Ala161Ser
XM_005255243.2:c.130G>T	XP_005255300.1:p.Ala44Ser
XM_011522453.1:c.481G>T	XP_011520755.1:p.Ala161Ser
XM_011522454.1:c.-144G>T	XP_011520756.1:n.-144G>T
NM_021646.3:c.481G>T	NP_067678.1:p.Ala161Ser
XM_005255243.4:c.130G>T	XP_005255300.1:p.Ala44Ser
XM_011522453.2:c.481G>T	XP_011520755.1:p.Ala161Ser
XM_011522454.3:c.-144G>T	XP_011520756.1:n.-144G>T
XM_017023121.2:c.-144G>T	XP_016878610.1:n.-144G>T
NM_001303450.2:c.481G>T	NP_001290379.1:p.Ala161Ser
NM_021646.4:c.481G>T MANE Select	NP_067678.1:p.Ala161Ser