Canonical Allele Identifier: CA12844712
Gene: ZFPM2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.105601093G>C , CM000670.2:g.105601093G>C GRCh38
NC_000008.10:g.106613321G>C , CM000670.1:g.106613321G>C GRCh37
NC_000008.9:g.106682497G>C NCBI36
NG_011723.1:g.287175G>C
NG_011723.2:g.287175G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000407775.7:c.421-33153G>C MANE Select ENSP00000384179.2:n.421-33153G>C
ENST00000407775.6:c.421-33153G>C ENSP00000384179.2:n.421-33153G>C
ENST00000511341.6:n.1161-33153G>C
ENST00000517361.1:c.25-33153G>C ENSP00000428720.1:n.25-33153G>C
ENST00000520027.5:c.25-33153G>C ENSP00000428149.1:n.25-33153G>C
ENST00000520492.5:c.25-33153G>C ENSP00000430757.1:n.25-33153G>C
NM_012082.3:c.421-33153G>C NP_036214.2:n.421-33153G>C
XM_011516946.1:c.460-33153G>C XP_011515248.1:n.460-33153G>C
XM_011516947.1:c.391-33153G>C XP_011515249.1:n.391-33153G>C
XM_011516948.1:c.262-33153G>C XP_011515250.1:n.262-33153G>C
XM_011516949.1:c.460-33153G>C XP_011515251.1:n.460-33153G>C
NM_001362836.1:c.262-33153G>C NP_001349765.1:n.262-33153G>C
NM_001362837.1:c.25-33153G>C NP_001349766.1:n.25-33153G>C
XM_011516947.3:c.391-33153G>C XP_011515249.1:n.391-33153G>C
NM_012082.4:c.421-33153G>C MANE Select NP_036214.2:n.421-33153G>C
NM_001362836.2:c.262-33153G>C NP_001349765.1:n.262-33153G>C
NM_001362837.2:c.25-33153G>C NP_001349766.1:n.25-33153G>C