Canonical Allele Identifier: CA1808195009
Gene: ZFPM2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.105503826C= , CM000670.2:g.105503826C= GRCh38
NC_000008.10:g.106516054C= , CM000670.1:g.106516054C= GRCh37
NC_000008.9:g.106585230C= NCBI36
NG_011723.1:g.189908C=
NG_011723.2:g.189908C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000407775.7:c.302-57537C= MANE Select ENSP00000384179.2:n.302-57537C=
ENST00000407775.6:c.302-57537C= ENSP00000384179.2:n.302-57537C=
ENST00000511341.6:n.1042-57537C=
ENST00000520027.5:c.-95-57537C= ENSP00000428149.1:n.-95-57537C=
ENST00000520492.5:c.-95-57537C= ENSP00000430757.1:n.-95-57537C=
ENST00000524235.5:n.515-57537C=
NM_012082.3:c.302-57537C= NP_036214.2:n.302-57537C=
XM_011516946.1:c.341-57537C= XP_011515248.1:n.341-57537C=
XM_011516947.1:c.272-57537C= XP_011515249.1:n.272-57537C=
XM_011516948.1:c.143-57537C= XP_011515250.1:n.143-57537C=
XM_011516949.1:c.341-57537C= XP_011515251.1:n.341-57537C=
NM_001362836.1:c.143-57537C= NP_001349765.1:n.143-57537C=
NM_001362837.1:c.-95-57537C= NP_001349766.1:n.-95-57537C=
XM_011516947.3:c.272-57537C= XP_011515249.1:n.272-57537C=
NM_012082.4:c.302-57537C= MANE Select NP_036214.2:n.302-57537C=
NM_001362836.2:c.143-57537C= NP_001349765.1:n.143-57537C=
NM_001362837.2:c.-95-57537C= NP_001349766.1:n.-95-57537C=