Canonical Allele Identifier: CA371952938
Gene: ZFPM2 HGNC NCBI
ZFPM2-AS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.105802108C>G , CM000670.2:g.105802108C>G GRCh38
NC_000008.10:g.106814336C>G , CM000670.1:g.106814336C>G GRCh37
NC_000008.9:g.106883512C>G NCBI36
NG_011723.1:g.488190C>G
NG_011723.2:g.488190C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000407775.7:c.2026C>G (ZFPM2) MANE Select ENSP00000384179.2:p.Pro676Ala
ENST00000407775.6:c.2026C>G (ZFPM2) ENSP00000384179.2:p.Pro676Ala
ENST00000517361.1:c.1630C>G (ZFPM2) ENSP00000428720.1:p.Pro544Ala
ENST00000520492.5:c.1630C>G (ZFPM2) ENSP00000430757.1:p.Pro544Ala
ENST00000522296.1:n.1820C>G (ZFPM2)
NM_012082.3:c.2026C>G (ZFPM2) NP_036214.2:p.Pro676Ala
NR_125796.1:n.180-3666G>C (ZFPM2-AS1)
NR_125797.1:n.191-3666G>C (ZFPM2-AS1)
XM_011516946.1:c.2065C>G (ZFPM2) XP_011515248.1:p.Pro689Ala
XM_011516947.1:c.1996C>G (ZFPM2) XP_011515249.1:p.Pro666Ala
XM_011516948.1:c.1867C>G (ZFPM2) XP_011515250.1:p.Pro623Ala
XM_011516949.1:c.1858C>G (ZFPM2) XP_011515251.1:p.Pro620Ala
NM_001362836.1:c.1867C>G (ZFPM2) NP_001349765.1:p.Pro623Ala
NM_001362837.1:c.1630C>G (ZFPM2) NP_001349766.1:p.Pro544Ala
XM_011516947.3:c.1996C>G (ZFPM2) XP_011515249.1:p.Pro666Ala
NM_012082.4:c.2026C>G (ZFPM2) MANE Select NP_036214.2:p.Pro676Ala
NM_001362836.2:c.1867C>G (ZFPM2) NP_001349765.1:p.Pro623Ala
NM_001362837.2:c.1630C>G (ZFPM2) NP_001349766.1:p.Pro544Ala