Canonical Allele Identifier: CA371946064
Gene: ZFPM2 HGNC NCBI
ZFPM2-AS1 HGNC NCBI
ClinVar RCV:
ClinVar Variation:
MyVariant.info:

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.105801128A>C , CM000670.2:g.105801128A>C GRCh38
NC_000008.10:g.106813356A>C , CM000670.1:g.106813356A>C GRCh37
NC_000008.9:g.106882532A>C NCBI36
NG_011723.1:g.487210A>C
NG_011723.2:g.487210A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000407775.7:c.1046A>C (ZFPM2) MANE Select ENSP00000384179.2:p.Asn349Thr
ENST00000407775.6:c.1046A>C (ZFPM2) ENSP00000384179.2:p.Asn349Thr
ENST00000517361.1:c.650A>C (ZFPM2) ENSP00000428720.1:p.Asn217Thr
ENST00000520492.5:c.650A>C (ZFPM2) ENSP00000430757.1:p.Asn217Thr
ENST00000522296.1:n.840A>C (ZFPM2)
NM_012082.3:c.1046A>C (ZFPM2) NP_036214.2:p.Asn349Thr
NR_125796.1:n.180-2686T>G (ZFPM2-AS1)
NR_125797.1:n.191-2686T>G (ZFPM2-AS1)
XM_011516946.1:c.1085A>C (ZFPM2) XP_011515248.1:p.Asn362Thr
XM_011516947.1:c.1016A>C (ZFPM2) XP_011515249.1:p.Asn339Thr
XM_011516948.1:c.887A>C (ZFPM2) XP_011515250.1:p.Asn296Thr
XM_011516949.1:c.878A>C (ZFPM2) XP_011515251.1:p.Asn293Thr
NM_001362836.1:c.887A>C (ZFPM2) NP_001349765.1:p.Asn296Thr
NM_001362837.1:c.650A>C (ZFPM2) NP_001349766.1:p.Asn217Thr
XM_011516947.3:c.1016A>C (ZFPM2) XP_011515249.1:p.Asn339Thr
NM_012082.4:c.1046A>C (ZFPM2) MANE Select NP_036214.2:p.Asn349Thr
NM_001362836.2:c.887A>C (ZFPM2) NP_001349765.1:p.Asn296Thr
NM_001362837.2:c.650A>C (ZFPM2) NP_001349766.1:p.Asn217Thr