Canonical Allele Identifier: CA462650204
Gene: ZFPM2 HGNC NCBI
ZFPM2-AS1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr8:g.106814065T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.105801837T>C , CM000670.2:g.105801837T>C GRCh38
NC_000008.10:g.106814065T>C , CM000670.1:g.106814065T>C GRCh37
NC_000008.9:g.106883241T>C NCBI36
NG_011723.1:g.487919T>C
NG_011723.2:g.487919T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000407775.7:c.1755T>C (ZFPM2) MANE Select ENSP00000384179.2:p.Pro585=
ENST00000407775.6:c.1755T>C (ZFPM2) ENSP00000384179.2:p.Pro585=
ENST00000517361.1:c.1359T>C (ZFPM2) ENSP00000428720.1:p.Pro453=
ENST00000520492.5:c.1359T>C (ZFPM2) ENSP00000430757.1:p.Pro453=
ENST00000522296.1:n.1549T>C (ZFPM2)
NM_012082.3:c.1755T>C (ZFPM2) NP_036214.2:p.Pro585=
NR_125796.1:n.180-3395A>G (ZFPM2-AS1)
NR_125797.1:n.191-3395A>G (ZFPM2-AS1)
XM_011516946.1:c.1794T>C (ZFPM2) XP_011515248.1:p.Pro598=
XM_011516947.1:c.1725T>C (ZFPM2) XP_011515249.1:p.Pro575=
XM_011516948.1:c.1596T>C (ZFPM2) XP_011515250.1:p.Pro532=
XM_011516949.1:c.1587T>C (ZFPM2) XP_011515251.1:p.Pro529=
NM_001362836.1:c.1596T>C (ZFPM2) NP_001349765.1:p.Pro532=
NM_001362837.1:c.1359T>C (ZFPM2) NP_001349766.1:p.Pro453=
XM_011516947.3:c.1725T>C (ZFPM2) XP_011515249.1:p.Pro575=
NM_012082.4:c.1755T>C (ZFPM2) MANE Select NP_036214.2:p.Pro585=
NM_001362836.2:c.1596T>C (ZFPM2) NP_001349765.1:p.Pro532=
NM_001362837.2:c.1359T>C (ZFPM2) NP_001349766.1:p.Pro453=