Canonical Allele Identifier: CA1808332084
Gene: ZFPM2 HGNC NCBI
ZFPM2-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.105801789T= , CM000670.2:g.105801789T= GRCh38
NC_000008.10:g.106814017T= , CM000670.1:g.106814017T= GRCh37
NC_000008.9:g.106883193T= NCBI36
NG_011723.1:g.487871T=
NG_011723.2:g.487871T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000407775.7:c.1707T= (ZFPM2) MANE Select ENSP00000384179.2:p.His569=
ENST00000407775.6:c.1707T= (ZFPM2) ENSP00000384179.2:p.His569=
ENST00000517361.1:c.1311T= (ZFPM2) ENSP00000428720.1:p.His437=
ENST00000520492.5:c.1311T= (ZFPM2) ENSP00000430757.1:p.His437=
ENST00000522296.1:n.1501T= (ZFPM2)
NM_012082.3:c.1707T= (ZFPM2) NP_036214.2:p.His569=
NR_125796.1:n.180-3347A= (ZFPM2-AS1)
NR_125797.1:n.191-3347A= (ZFPM2-AS1)
XM_011516946.1:c.1746T= (ZFPM2) XP_011515248.1:p.His582=
XM_011516947.1:c.1677T= (ZFPM2) XP_011515249.1:p.His559=
XM_011516948.1:c.1548T= (ZFPM2) XP_011515250.1:p.His516=
XM_011516949.1:c.1539T= (ZFPM2) XP_011515251.1:p.His513=
NM_001362836.1:c.1548T= (ZFPM2) NP_001349765.1:p.His516=
NM_001362837.1:c.1311T= (ZFPM2) NP_001349766.1:p.His437=
XM_011516947.3:c.1677T= (ZFPM2) XP_011515249.1:p.His559=
NM_012082.4:c.1707T= (ZFPM2) MANE Select NP_036214.2:p.His569=
NM_001362836.2:c.1548T= (ZFPM2) NP_001349765.1:p.His516=
NM_001362837.2:c.1311T= (ZFPM2) NP_001349766.1:p.His437=