Canonical Allele Identifier: CA1808159233

Gene: ZFPM2

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.105419192A= , CM000670.2:g.105419192A=	GRCh38
NC_000008.10:g.106431420A= , CM000670.1:g.106431420A=	GRCh37
NC_000008.9:g.106500596A=	NCBI36
NG_011723.1:g.105274A=
NG_011723.2:g.105274A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000407775.7:c.89A= MANE Select	ENSP00000384179.2:p.Glu30=
ENST00000407775.6:c.89A=	ENSP00000384179.2:p.Glu30=
ENST00000511341.6:n.829A=
ENST00000518180.1:n.528A=
ENST00000520027.5:c.-308A=	ENSP00000428149.1:n.-308A=
ENST00000520492.5:c.-308A=	ENSP00000430757.1:n.-308A=
ENST00000522160.1:n.49A=
ENST00000524235.5:n.302A=
NM_012082.3:c.89A=	NP_036214.2:p.Glu30=
XM_011516946.1:c.128A=	XP_011515248.1:p.Glu43=
XM_011516947.1:c.59A=	XP_011515249.1:p.Glu20=
XM_011516948.1:c.41-25088A=	XP_011515250.1:n.41-25088A=
XM_011516949.1:c.128A=	XP_011515251.1:p.Glu43=
NM_001362836.1:c.41-25088A=	NP_001349765.1:n.41-25088A=
NM_001362837.1:c.-308A=	NP_001349766.1:n.-308A=
XM_011516947.3:c.59A=	XP_011515249.1:p.Glu20=
NM_012082.4:c.89A= MANE Select	NP_036214.2:p.Glu30=
NM_001362836.2:c.41-25088A=	NP_001349765.1:n.41-25088A=
NM_001362837.2:c.-308A=	NP_001349766.1:n.-308A=