Canonical Allele Identifier: CA462650006

Gene: ZFPM2 ZFPM2-AS1

Linked Data

• MyVariant Identifiers: chr8:g.106813849T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.105801621T>G , CM000670.2:g.105801621T>G	GRCh38
NC_000008.10:g.106813849T>G , CM000670.1:g.106813849T>G	GRCh37
NC_000008.9:g.106883025T>G	NCBI36
NG_011723.1:g.487703T>G
NG_011723.2:g.487703T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000407775.7:c.1539T>G (ZFPM2) MANE Select	ENSP00000384179.2:p.Ala513=
ENST00000407775.6:c.1539T>G (ZFPM2)	ENSP00000384179.2:p.Ala513=
ENST00000517361.1:c.1143T>G (ZFPM2)	ENSP00000428720.1:p.Ala381=
ENST00000520492.5:c.1143T>G (ZFPM2)	ENSP00000430757.1:p.Ala381=
ENST00000522296.1:n.1333T>G (ZFPM2)
NM_012082.3:c.1539T>G (ZFPM2)	NP_036214.2:p.Ala513=
NR_125796.1:n.180-3179A>C (ZFPM2-AS1)
NR_125797.1:n.191-3179A>C (ZFPM2-AS1)
XM_011516946.1:c.1578T>G (ZFPM2)	XP_011515248.1:p.Ala526=
XM_011516947.1:c.1509T>G (ZFPM2)	XP_011515249.1:p.Ala503=
XM_011516948.1:c.1380T>G (ZFPM2)	XP_011515250.1:p.Ala460=
XM_011516949.1:c.1371T>G (ZFPM2)	XP_011515251.1:p.Ala457=
NM_001362836.1:c.1380T>G (ZFPM2)	NP_001349765.1:p.Ala460=
NM_001362837.1:c.1143T>G (ZFPM2)	NP_001349766.1:p.Ala381=
XM_011516947.3:c.1509T>G (ZFPM2)	XP_011515249.1:p.Ala503=
NM_012082.4:c.1539T>G (ZFPM2) MANE Select	NP_036214.2:p.Ala513=
NM_001362836.2:c.1380T>G (ZFPM2)	NP_001349765.1:p.Ala460=
NM_001362837.2:c.1143T>G (ZFPM2)	NP_001349766.1:p.Ala381=