Canonical Allele Identifier: CA1808163421
Gene: ZFPM2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.105437414A= , CM000670.2:g.105437414A= GRCh38
NC_000008.10:g.106449642A= , CM000670.1:g.106449642A= GRCh37
NC_000008.9:g.106518818A= NCBI36
NG_011723.1:g.123496A=
NG_011723.2:g.123496A=

Transcript Alleles

HGVS Amino-acid change
ENST00000407775.7:c.200-6866A= MANE Select ENSP00000384179.2:n.200-6866A=
ENST00000407775.6:c.200-6866A= ENSP00000384179.2:n.200-6866A=
ENST00000511341.6:n.940-6866A=
ENST00000520027.5:c.-197-6866A= ENSP00000428149.1:n.-197-6866A=
ENST00000520492.5:c.-197-6866A= ENSP00000430757.1:n.-197-6866A=
ENST00000522160.1:n.160-6866A=
ENST00000524235.5:n.413-6866A=
NM_012082.3:c.200-6866A= NP_036214.2:n.200-6866A=
XM_011516946.1:c.239-6866A= XP_011515248.1:n.239-6866A=
XM_011516947.1:c.170-6866A= XP_011515249.1:n.170-6866A=
XM_011516948.1:c.41-6866A= XP_011515250.1:n.41-6866A=
XM_011516949.1:c.239-6866A= XP_011515251.1:n.239-6866A=
NM_001362836.1:c.41-6866A= NP_001349765.1:n.41-6866A=
NM_001362837.1:c.-197-6866A= NP_001349766.1:n.-197-6866A=
XM_011516947.3:c.170-6866A= XP_011515249.1:n.170-6866A=
NM_012082.4:c.200-6866A= MANE Select NP_036214.2:n.200-6866A=
NM_001362836.2:c.41-6866A= NP_001349765.1:n.41-6866A=
NM_001362837.2:c.-197-6866A= NP_001349766.1:n.-197-6866A=