Canonical Allele Identifier: CA1808332039
Gene: ZFPM2 HGNC NCBI
ZFPM2-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.105801685T= , CM000670.2:g.105801685T= GRCh38
NC_000008.10:g.106813913T= , CM000670.1:g.106813913T= GRCh37
NC_000008.9:g.106883089T= NCBI36
NG_011723.1:g.487767T=
NG_011723.2:g.487767T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000407775.7:c.1603T= (ZFPM2) MANE Select ENSP00000384179.2:p.Tyr535=
ENST00000407775.6:c.1603T= (ZFPM2) ENSP00000384179.2:p.Tyr535=
ENST00000517361.1:c.1207T= (ZFPM2) ENSP00000428720.1:p.Tyr403=
ENST00000520492.5:c.1207T= (ZFPM2) ENSP00000430757.1:p.Tyr403=
ENST00000522296.1:n.1397T= (ZFPM2)
NM_012082.3:c.1603T= (ZFPM2) NP_036214.2:p.Tyr535=
NR_125796.1:n.180-3243A= (ZFPM2-AS1)
NR_125797.1:n.191-3243A= (ZFPM2-AS1)
XM_011516946.1:c.1642T= (ZFPM2) XP_011515248.1:p.Tyr548=
XM_011516947.1:c.1573T= (ZFPM2) XP_011515249.1:p.Tyr525=
XM_011516948.1:c.1444T= (ZFPM2) XP_011515250.1:p.Tyr482=
XM_011516949.1:c.1435T= (ZFPM2) XP_011515251.1:p.Tyr479=
NM_001362836.1:c.1444T= (ZFPM2) NP_001349765.1:p.Tyr482=
NM_001362837.1:c.1207T= (ZFPM2) NP_001349766.1:p.Tyr403=
XM_011516947.3:c.1573T= (ZFPM2) XP_011515249.1:p.Tyr525=
NM_012082.4:c.1603T= (ZFPM2) MANE Select NP_036214.2:p.Tyr535=
NM_001362836.2:c.1444T= (ZFPM2) NP_001349765.1:p.Tyr482=
NM_001362837.2:c.1207T= (ZFPM2) NP_001349766.1:p.Tyr403=