Canonical Allele Identifier: CA371952926
Gene: ZFPM2 HGNC NCBI
ZFPM2-AS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 3045797
ClinVar RCV Id: RCV003934425
dbSNP Id: rs1400566117

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.105802103G>A , CM000670.2:g.105802103G>A GRCh38
NC_000008.10:g.106814331G>A , CM000670.1:g.106814331G>A GRCh37
NC_000008.9:g.106883507G>A NCBI36
NG_011723.1:g.488185G>A
NG_011723.2:g.488185G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000407775.7:c.2021G>A (ZFPM2) MANE Select ENSP00000384179.2:p.Ser674Asn
ENST00000407775.6:c.2021G>A (ZFPM2) ENSP00000384179.2:p.Ser674Asn
ENST00000517361.1:c.1625G>A (ZFPM2) ENSP00000428720.1:p.Ser542Asn
ENST00000520492.5:c.1625G>A (ZFPM2) ENSP00000430757.1:p.Ser542Asn
ENST00000522296.1:n.1815G>A (ZFPM2)
NM_012082.3:c.2021G>A (ZFPM2) NP_036214.2:p.Ser674Asn
NR_125796.1:n.180-3661C>T (ZFPM2-AS1)
NR_125797.1:n.191-3661C>T (ZFPM2-AS1)
XM_011516946.1:c.2060G>A (ZFPM2) XP_011515248.1:p.Ser687Asn
XM_011516947.1:c.1991G>A (ZFPM2) XP_011515249.1:p.Ser664Asn
XM_011516948.1:c.1862G>A (ZFPM2) XP_011515250.1:p.Ser621Asn
XM_011516949.1:c.1853G>A (ZFPM2) XP_011515251.1:p.Ser618Asn
NM_001362836.1:c.1862G>A (ZFPM2) NP_001349765.1:p.Ser621Asn
NM_001362837.1:c.1625G>A (ZFPM2) NP_001349766.1:p.Ser542Asn
XM_011516947.3:c.1991G>A (ZFPM2) XP_011515249.1:p.Ser664Asn
NM_012082.4:c.2021G>A (ZFPM2) MANE Select NP_036214.2:p.Ser674Asn
NM_001362836.2:c.1862G>A (ZFPM2) NP_001349765.1:p.Ser621Asn
NM_001362837.2:c.1625G>A (ZFPM2) NP_001349766.1:p.Ser542Asn