Canonical Allele Identifier: CA372025623

Gene: ZFPM2

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000407775.7:c.89A>C MANE Select	ENSP00000384179.2:p.Glu30Ala
ENST00000407775.6:c.89A>C	ENSP00000384179.2:p.Glu30Ala
ENST00000511341.6:n.829A>C
ENST00000518180.1:n.528A>C
ENST00000520027.5:c.-308A>C	ENSP00000428149.1:n.-308A>C
ENST00000520492.5:c.-308A>C	ENSP00000430757.1:n.-308A>C
ENST00000522160.1:n.49A>C
ENST00000524235.5:n.302A>C
NM_012082.3:c.89A>C	NP_036214.2:p.Glu30Ala
XM_011516946.1:c.128A>C	XP_011515248.1:p.Glu43Ala
XM_011516947.1:c.59A>C	XP_011515249.1:p.Glu20Ala
XM_011516948.1:c.41-25088A>C	XP_011515250.1:n.41-25088A>C
XM_011516949.1:c.128A>C	XP_011515251.1:p.Glu43Ala
NM_001362836.1:c.41-25088A>C	NP_001349765.1:n.41-25088A>C
NM_001362837.1:c.-308A>C	NP_001349766.1:n.-308A>C
XM_011516947.3:c.59A>C	XP_011515249.1:p.Glu20Ala
NM_012082.4:c.89A>C MANE Select	NP_036214.2:p.Glu30Ala
NM_001362836.2:c.41-25088A>C	NP_001349765.1:n.41-25088A>C
NM_001362837.2:c.-308A>C	NP_001349766.1:n.-308A>C