Canonical Allele Identifier: CA371950892

Gene: ZFPM2 ZFPM2-AS1

Linked Data

• gnomAD v4: 8-105801590-T-G
• MyVariant Identifiers: chr8:g.106813818T>G (hg19) ; chr8:g.105801590T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.105801590T>G , CM000670.2:g.105801590T>G	GRCh38
NC_000008.10:g.106813818T>G , CM000670.1:g.106813818T>G	GRCh37
NC_000008.9:g.106882994T>G	NCBI36
NG_011723.1:g.487672T>G
NG_011723.2:g.487672T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000407775.7:c.1508T>G (ZFPM2) MANE Select	ENSP00000384179.2:p.Phe503Cys
ENST00000407775.6:c.1508T>G (ZFPM2)	ENSP00000384179.2:p.Phe503Cys
ENST00000517361.1:c.1112T>G (ZFPM2)	ENSP00000428720.1:p.Phe371Cys
ENST00000520492.5:c.1112T>G (ZFPM2)	ENSP00000430757.1:p.Phe371Cys
ENST00000522296.1:n.1302T>G (ZFPM2)
NM_012082.3:c.1508T>G (ZFPM2)	NP_036214.2:p.Phe503Cys
NR_125796.1:n.180-3148A>C (ZFPM2-AS1)
NR_125797.1:n.191-3148A>C (ZFPM2-AS1)
XM_011516946.1:c.1547T>G (ZFPM2)	XP_011515248.1:p.Phe516Cys
XM_011516947.1:c.1478T>G (ZFPM2)	XP_011515249.1:p.Phe493Cys
XM_011516948.1:c.1349T>G (ZFPM2)	XP_011515250.1:p.Phe450Cys
XM_011516949.1:c.1340T>G (ZFPM2)	XP_011515251.1:p.Phe447Cys
NM_001362836.1:c.1349T>G (ZFPM2)	NP_001349765.1:p.Phe450Cys
NM_001362837.1:c.1112T>G (ZFPM2)	NP_001349766.1:p.Phe371Cys
XM_011516947.3:c.1478T>G (ZFPM2)	XP_011515249.1:p.Phe493Cys
NM_012082.4:c.1508T>G (ZFPM2) MANE Select	NP_036214.2:p.Phe503Cys
NM_001362836.2:c.1349T>G (ZFPM2)	NP_001349765.1:p.Phe450Cys
NM_001362837.2:c.1112T>G (ZFPM2)	NP_001349766.1:p.Phe371Cys