Canonical Allele Identifier: CA371951839

Gene: ZFPM2 ZFPM2-AS1

Linked Data

• MyVariant Identifiers: chr8:g.106813995A>G (hg19) ; chr8:g.105801767A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.105801767A>G , CM000670.2:g.105801767A>G	GRCh38
NC_000008.10:g.106813995A>G , CM000670.1:g.106813995A>G	GRCh37
NC_000008.9:g.106883171A>G	NCBI36
NG_011723.1:g.487849A>G
NG_011723.2:g.487849A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000407775.7:c.1685A>G (ZFPM2) MANE Select	ENSP00000384179.2:p.Asn562Ser
ENST00000407775.6:c.1685A>G (ZFPM2)	ENSP00000384179.2:p.Asn562Ser
ENST00000517361.1:c.1289A>G (ZFPM2)	ENSP00000428720.1:p.Asn430Ser
ENST00000520492.5:c.1289A>G (ZFPM2)	ENSP00000430757.1:p.Asn430Ser
ENST00000522296.1:n.1479A>G (ZFPM2)
NM_012082.3:c.1685A>G (ZFPM2)	NP_036214.2:p.Asn562Ser
NR_125796.1:n.180-3325T>C (ZFPM2-AS1)
NR_125797.1:n.191-3325T>C (ZFPM2-AS1)
XM_011516946.1:c.1724A>G (ZFPM2)	XP_011515248.1:p.Asn575Ser
XM_011516947.1:c.1655A>G (ZFPM2)	XP_011515249.1:p.Asn552Ser
XM_011516948.1:c.1526A>G (ZFPM2)	XP_011515250.1:p.Asn509Ser
XM_011516949.1:c.1517A>G (ZFPM2)	XP_011515251.1:p.Asn506Ser
NM_001362836.1:c.1526A>G (ZFPM2)	NP_001349765.1:p.Asn509Ser
NM_001362837.1:c.1289A>G (ZFPM2)	NP_001349766.1:p.Asn430Ser
XM_011516947.3:c.1655A>G (ZFPM2)	XP_011515249.1:p.Asn552Ser
NM_012082.4:c.1685A>G (ZFPM2) MANE Select	NP_036214.2:p.Asn562Ser
NM_001362836.2:c.1526A>G (ZFPM2)	NP_001349765.1:p.Asn509Ser
NM_001362837.2:c.1289A>G (ZFPM2)	NP_001349766.1:p.Asn430Ser