Canonical Allele Identifier: CA462650085

Gene: ZFPM2 ZFPM2-AS1

Linked Data

• dbSNP Id: rs1814022833
• MyVariant Identifiers: chr8:g.106813924C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.105801696C>A , CM000670.2:g.105801696C>A	GRCh38
NC_000008.10:g.106813924C>A , CM000670.1:g.106813924C>A	GRCh37
NC_000008.9:g.106883100C>A	NCBI36
NG_011723.1:g.487778C>A
NG_011723.2:g.487778C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000407775.7:c.1614C>A (ZFPM2) MANE Select	ENSP00000384179.2:p.Val538=
ENST00000407775.6:c.1614C>A (ZFPM2)	ENSP00000384179.2:p.Val538=
ENST00000517361.1:c.1218C>A (ZFPM2)	ENSP00000428720.1:p.Val406=
ENST00000520492.5:c.1218C>A (ZFPM2)	ENSP00000430757.1:p.Val406=
ENST00000522296.1:n.1408C>A (ZFPM2)
NM_012082.3:c.1614C>A (ZFPM2)	NP_036214.2:p.Val538=
NR_125796.1:n.180-3254G>T (ZFPM2-AS1)
NR_125797.1:n.191-3254G>T (ZFPM2-AS1)
XM_011516946.1:c.1653C>A (ZFPM2)	XP_011515248.1:p.Val551=
XM_011516947.1:c.1584C>A (ZFPM2)	XP_011515249.1:p.Val528=
XM_011516948.1:c.1455C>A (ZFPM2)	XP_011515250.1:p.Val485=
XM_011516949.1:c.1446C>A (ZFPM2)	XP_011515251.1:p.Val482=
NM_001362836.1:c.1455C>A (ZFPM2)	NP_001349765.1:p.Val485=
NM_001362837.1:c.1218C>A (ZFPM2)	NP_001349766.1:p.Val406=
XM_011516947.3:c.1584C>A (ZFPM2)	XP_011515249.1:p.Val528=
NM_012082.4:c.1614C>A (ZFPM2) MANE Select	NP_036214.2:p.Val538=
NM_001362836.2:c.1455C>A (ZFPM2)	NP_001349765.1:p.Val485=
NM_001362837.2:c.1218C>A (ZFPM2)	NP_001349766.1:p.Val406=