Canonical Allele Identifier: CA1808192075
Gene: ZFPM2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.105497708C= , CM000670.2:g.105497708C= GRCh38
NC_000008.10:g.106509936C= , CM000670.1:g.106509936C= GRCh37
NC_000008.9:g.106579112C= NCBI36
NG_011723.1:g.183790C=
NG_011723.2:g.183790C=

Transcript Alleles

HGVS Amino-acid change
ENST00000407775.7:c.301+53327C= MANE Select ENSP00000384179.2:n.301+53327C=
ENST00000407775.6:c.301+53327C= ENSP00000384179.2:n.301+53327C=
ENST00000511341.6:n.1041+53327C=
ENST00000520027.5:c.-96+53327C= ENSP00000428149.1:n.-96+53327C=
ENST00000520492.5:c.-96+53327C= ENSP00000430757.1:n.-96+53327C=
ENST00000524235.5:n.514+53327C=
NM_012082.3:c.301+53327C= NP_036214.2:n.301+53327C=
XM_011516946.1:c.340+53327C= XP_011515248.1:n.340+53327C=
XM_011516947.1:c.271+53327C= XP_011515249.1:n.271+53327C=
XM_011516948.1:c.142+53327C= XP_011515250.1:n.142+53327C=
XM_011516949.1:c.340+53327C= XP_011515251.1:n.340+53327C=
NM_001362836.1:c.142+53327C= NP_001349765.1:n.142+53327C=
NM_001362837.1:c.-96+53327C= NP_001349766.1:n.-96+53327C=
XM_011516947.3:c.271+53327C= XP_011515249.1:n.271+53327C=
NM_012082.4:c.301+53327C= MANE Select NP_036214.2:n.301+53327C=
NM_001362836.2:c.142+53327C= NP_001349765.1:n.142+53327C=
NM_001362837.2:c.-96+53327C= NP_001349766.1:n.-96+53327C=