Canonical Allele Identifier: CA493315914

Gene: ZNF500

Linked Data

• gnomAD v4: 16-4762298-G-C
• MyVariant Identifiers: chr16:g.4812299G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.4762298G>C , CM000678.2:g.4762298G>C	GRCh38
NC_000016.9:g.4812299G>C , CM000678.1:g.4812299G>C	GRCh37
NC_000016.8:g.4752300G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000219478.11:c.636C>G MANE Select	ENSP00000219478.5:p.Ala212=
ENST00000219478.10:c.636C>G	ENSP00000219478.5:p.Ala212=
ENST00000545009.1:c.636C>G	ENSP00000445714.1:p.Ala212=
ENST00000589422.1:c.*164C>G	ENSP00000466375.1:n.*164C>G
NM_001303450.1:c.636C>G	NP_001290379.1:p.Ala212=
NM_021646.2:c.636C>G	NP_067678.1:p.Ala212=
XM_005255243.2:c.285C>G	XP_005255300.1:p.Ala95=
XM_011522453.1:c.636C>G	XP_011520755.1:p.Ala212=
XM_011522454.1:c.12C>G	XP_011520756.1:p.Ala4=
NM_021646.3:c.636C>G	NP_067678.1:p.Ala212=
XM_005255243.4:c.285C>G	XP_005255300.1:p.Ala95=
XM_011522453.2:c.636C>G	XP_011520755.1:p.Ala212=
XM_011522454.3:c.12C>G	XP_011520756.1:p.Ala4=
XM_017023121.2:c.12C>G	XP_016878610.1:p.Ala4=
NM_001303450.2:c.636C>G	NP_001290379.1:p.Ala212=
NM_021646.4:c.636C>G MANE Select	NP_067678.1:p.Ala212=