Canonical Allele Identifier: CA170936

Gene: ZFPM2 ZFPM2-AS1

Linked Data

• ClinVar Variation Id: 156583
• ClinVar RCV Id: RCV000144724
• dbSNP Id: rs606231252
• MyVariant Identifiers: chr8:g.106813516T>A (hg19) ; chr8:g.105801288T>A (hg38)
• PubMed: PMID:24549039

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.105801288T>A , CM000670.2:g.105801288T>A	GRCh38
NC_000008.10:g.106813516T>A , CM000670.1:g.106813516T>A	GRCh37
NC_000008.9:g.106882692T>A	NCBI36
NG_011723.1:g.487370T>A
NG_011723.2:g.487370T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000407775.7:c.1206T>A (ZFPM2) MANE Select	ENSP00000384179.2:p.Ser402Arg
ENST00000407775.6:c.1206T>A (ZFPM2)	ENSP00000384179.2:p.Ser402Arg
ENST00000517361.1:c.810T>A (ZFPM2)	ENSP00000428720.1:p.Ser270Arg
ENST00000520492.5:c.810T>A (ZFPM2)	ENSP00000430757.1:p.Ser270Arg
ENST00000522296.1:n.1000T>A (ZFPM2)
NM_012082.3:c.1206T>A (ZFPM2)	NP_036214.2:p.Ser402Arg
NR_125796.1:n.180-2846A>T (ZFPM2-AS1)
NR_125797.1:n.191-2846A>T (ZFPM2-AS1)
XM_011516946.1:c.1245T>A (ZFPM2)	XP_011515248.1:p.Ser415Arg
XM_011516947.1:c.1176T>A (ZFPM2)	XP_011515249.1:p.Ser392Arg
XM_011516948.1:c.1047T>A (ZFPM2)	XP_011515250.1:p.Ser349Arg
XM_011516949.1:c.1038T>A (ZFPM2)	XP_011515251.1:p.Ser346Arg
NM_001362836.1:c.1047T>A (ZFPM2)	NP_001349765.1:p.Ser349Arg
NM_001362837.1:c.810T>A (ZFPM2)	NP_001349766.1:p.Ser270Arg
XM_011516947.3:c.1176T>A (ZFPM2)	XP_011515249.1:p.Ser392Arg
NM_012082.4:c.1206T>A (ZFPM2) MANE Select	NP_036214.2:p.Ser402Arg
NM_001362836.2:c.1047T>A (ZFPM2)	NP_001349765.1:p.Ser349Arg
NM_001362837.2:c.810T>A (ZFPM2)	NP_001349766.1:p.Ser270Arg