Canonical Allele Identifier: CA2717952701
Gene: ZFPM2 HGNC NCBI

Linked Data

dbSNP Id: rs2130174676

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.105437495_105437500del , CM000670.2:g.105437495_105437500del GRCh38
NC_000008.10:g.106449723_106449728del , CM000670.1:g.106449723_106449728del GRCh37
NC_000008.9:g.106518899_106518904del NCBI36
NG_011723.1:g.123577_123582del
NG_011723.2:g.123577_123582del

Transcript Alleles

HGVS Amino-acid Change
ENST00000407775.7:c.200-6785_200-6780del MANE Select ENSP00000384179.2:n.200-6785_200-6780del
ENST00000407775.6:c.200-6785_200-6780del ENSP00000384179.2:n.200-6785_200-6780del
ENST00000511341.6:n.940-6785_940-6780del
ENST00000520027.5:c.-197-6785_-197-6780del ENSP00000428149.1:n.-197-6785_-197-6780del
ENST00000520492.5:c.-197-6785_-197-6780del ENSP00000430757.1:n.-197-6785_-197-6780del
ENST00000522160.1:n.160-6785_160-6780del
ENST00000524235.5:n.413-6785_413-6780del
NM_012082.3:c.200-6785_200-6780del NP_036214.2:n.200-6785_200-6780del
XM_011516946.1:c.239-6785_239-6780del XP_011515248.1:n.239-6785_239-6780del
XM_011516947.1:c.170-6785_170-6780del XP_011515249.1:n.170-6785_170-6780del
XM_011516948.1:c.41-6785_41-6780del XP_011515250.1:n.41-6785_41-6780del
XM_011516949.1:c.239-6785_239-6780del XP_011515251.1:n.239-6785_239-6780del
NM_001362836.1:c.41-6785_41-6780del NP_001349765.1:n.41-6785_41-6780del
NM_001362837.1:c.-197-6785_-197-6780del NP_001349766.1:n.-197-6785_-197-6780del
XM_011516947.3:c.170-6785_170-6780del XP_011515249.1:n.170-6785_170-6780del
NM_012082.4:c.200-6785_200-6780del MANE Select NP_036214.2:n.200-6785_200-6780del
NM_001362836.2:c.41-6785_41-6780del NP_001349765.1:n.41-6785_41-6780del
NM_001362837.2:c.-197-6785_-197-6780del NP_001349766.1:n.-197-6785_-197-6780del