Canonical Allele Identifier: CA462650076
Gene: ZFPM2 HGNC NCBI
ZFPM2-AS1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr8:g.106814188C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.105801960C>A , CM000670.2:g.105801960C>A GRCh38
NC_000008.10:g.106814188C>A , CM000670.1:g.106814188C>A GRCh37
NC_000008.9:g.106883364C>A NCBI36
NG_011723.1:g.488042C>A
NG_011723.2:g.488042C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000407775.7:c.1878C>A (ZFPM2) MANE Select ENSP00000384179.2:p.Ile626=
ENST00000407775.6:c.1878C>A (ZFPM2) ENSP00000384179.2:p.Ile626=
ENST00000517361.1:c.1482C>A (ZFPM2) ENSP00000428720.1:p.Ile494=
ENST00000520492.5:c.1482C>A (ZFPM2) ENSP00000430757.1:p.Ile494=
ENST00000522296.1:n.1672C>A (ZFPM2)
NM_012082.3:c.1878C>A (ZFPM2) NP_036214.2:p.Ile626=
NR_125796.1:n.180-3518G>T (ZFPM2-AS1)
NR_125797.1:n.191-3518G>T (ZFPM2-AS1)
XM_011516946.1:c.1917C>A (ZFPM2) XP_011515248.1:p.Ile639=
XM_011516947.1:c.1848C>A (ZFPM2) XP_011515249.1:p.Ile616=
XM_011516948.1:c.1719C>A (ZFPM2) XP_011515250.1:p.Ile573=
XM_011516949.1:c.1710C>A (ZFPM2) XP_011515251.1:p.Ile570=
NM_001362836.1:c.1719C>A (ZFPM2) NP_001349765.1:p.Ile573=
NM_001362837.1:c.1482C>A (ZFPM2) NP_001349766.1:p.Ile494=
XM_011516947.3:c.1848C>A (ZFPM2) XP_011515249.1:p.Ile616=
NM_012082.4:c.1878C>A (ZFPM2) MANE Select NP_036214.2:p.Ile626=
NM_001362836.2:c.1719C>A (ZFPM2) NP_001349765.1:p.Ile573=
NM_001362837.2:c.1482C>A (ZFPM2) NP_001349766.1:p.Ile494=