Canonical Allele Identifier: CA462649994
Gene: ZFPM2 HGNC NCBI
ZFPM2-AS1 HGNC NCBI

Linked Data

COSMIC: COSM387922
MyVariant Identifiers: chr8:g.106813834C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.105801606C>A , CM000670.2:g.105801606C>A GRCh38
NC_000008.10:g.106813834C>A , CM000670.1:g.106813834C>A GRCh37
NC_000008.9:g.106883010C>A NCBI36
NG_011723.1:g.487688C>A
NG_011723.2:g.487688C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000407775.7:c.1524C>A (ZFPM2) MANE Select ENSP00000384179.2:p.Thr508=
ENST00000407775.6:c.1524C>A (ZFPM2) ENSP00000384179.2:p.Thr508=
ENST00000517361.1:c.1128C>A (ZFPM2) ENSP00000428720.1:p.Thr376=
ENST00000520492.5:c.1128C>A (ZFPM2) ENSP00000430757.1:p.Thr376=
ENST00000522296.1:n.1318C>A (ZFPM2)
NM_012082.3:c.1524C>A (ZFPM2) NP_036214.2:p.Thr508=
NR_125796.1:n.180-3164G>T (ZFPM2-AS1)
NR_125797.1:n.191-3164G>T (ZFPM2-AS1)
XM_011516946.1:c.1563C>A (ZFPM2) XP_011515248.1:p.Thr521=
XM_011516947.1:c.1494C>A (ZFPM2) XP_011515249.1:p.Thr498=
XM_011516948.1:c.1365C>A (ZFPM2) XP_011515250.1:p.Thr455=
XM_011516949.1:c.1356C>A (ZFPM2) XP_011515251.1:p.Thr452=
NM_001362836.1:c.1365C>A (ZFPM2) NP_001349765.1:p.Thr455=
NM_001362837.1:c.1128C>A (ZFPM2) NP_001349766.1:p.Thr376=
XM_011516947.3:c.1494C>A (ZFPM2) XP_011515249.1:p.Thr498=
NM_012082.4:c.1524C>A (ZFPM2) MANE Select NP_036214.2:p.Thr508=
NM_001362836.2:c.1365C>A (ZFPM2) NP_001349765.1:p.Thr455=
NM_001362837.2:c.1128C>A (ZFPM2) NP_001349766.1:p.Thr376=