Canonical Allele Identifier: CA371951155
Gene: ZFPM2 HGNC NCBI
ZFPM2-AS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.105801668G>C , CM000670.2:g.105801668G>C GRCh38
NC_000008.10:g.106813896G>C , CM000670.1:g.106813896G>C GRCh37
NC_000008.9:g.106883072G>C NCBI36
NG_011723.1:g.487750G>C
NG_011723.2:g.487750G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000407775.7:c.1586G>C (ZFPM2) MANE Select ENSP00000384179.2:p.Arg529Thr
ENST00000407775.6:c.1586G>C (ZFPM2) ENSP00000384179.2:p.Arg529Thr
ENST00000517361.1:c.1190G>C (ZFPM2) ENSP00000428720.1:p.Arg397Thr
ENST00000520492.5:c.1190G>C (ZFPM2) ENSP00000430757.1:p.Arg397Thr
ENST00000522296.1:n.1380G>C (ZFPM2)
NM_012082.3:c.1586G>C (ZFPM2) NP_036214.2:p.Arg529Thr
NR_125796.1:n.180-3226C>G (ZFPM2-AS1)
NR_125797.1:n.191-3226C>G (ZFPM2-AS1)
XM_011516946.1:c.1625G>C (ZFPM2) XP_011515248.1:p.Arg542Thr
XM_011516947.1:c.1556G>C (ZFPM2) XP_011515249.1:p.Arg519Thr
XM_011516948.1:c.1427G>C (ZFPM2) XP_011515250.1:p.Arg476Thr
XM_011516949.1:c.1418G>C (ZFPM2) XP_011515251.1:p.Arg473Thr
NM_001362836.1:c.1427G>C (ZFPM2) NP_001349765.1:p.Arg476Thr
NM_001362837.1:c.1190G>C (ZFPM2) NP_001349766.1:p.Arg397Thr
XM_011516947.3:c.1556G>C (ZFPM2) XP_011515249.1:p.Arg519Thr
NM_012082.4:c.1586G>C (ZFPM2) MANE Select NP_036214.2:p.Arg529Thr
NM_001362836.2:c.1427G>C (ZFPM2) NP_001349765.1:p.Arg476Thr
NM_001362837.2:c.1190G>C (ZFPM2) NP_001349766.1:p.Arg397Thr