Canonical Allele Identifier: CA493316242

Gene: ZNF500

Linked Data

• gnomAD v4: 16-4762754-G-A
• MyVariant Identifiers: chr16:g.4812755G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.4762754G>A , CM000678.2:g.4762754G>A	GRCh38
NC_000016.9:g.4812755G>A , CM000678.1:g.4812755G>A	GRCh37
NC_000016.8:g.4752756G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000219478.11:c.417C>T MANE Select	ENSP00000219478.5:p.Gly139=
ENST00000219478.10:c.417C>T	ENSP00000219478.5:p.Gly139=
ENST00000545009.1:c.417C>T	ENSP00000445714.1:p.Gly139=
ENST00000589422.1:c.415-41C>T	ENSP00000466375.1:n.415-41C>T
NM_001303450.1:c.417C>T	NP_001290379.1:p.Gly139=
NM_021646.2:c.417C>T	NP_067678.1:p.Gly139=
XM_005255243.2:c.66C>T	XP_005255300.1:p.Gly22=
XM_011522453.1:c.417C>T	XP_011520755.1:p.Gly139=
XM_011522454.1:c.-167-41C>T	XP_011520756.1:n.-167-41C>T
NM_021646.3:c.417C>T	NP_067678.1:p.Gly139=
XM_005255243.4:c.66C>T	XP_005255300.1:p.Gly22=
XM_011522453.2:c.417C>T	XP_011520755.1:p.Gly139=
XM_011522454.3:c.-167-41C>T	XP_011520756.1:n.-167-41C>T
XM_017023121.2:c.-208C>T	XP_016878610.1:n.-208C>T
NM_001303450.2:c.417C>T	NP_001290379.1:p.Gly139=
NM_021646.4:c.417C>T MANE Select	NP_067678.1:p.Gly139=