Canonical Allele Identifier: CA1808222354

Gene: ZFPM2

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.105561395C= , CM000670.2:g.105561395C=	GRCh38
NC_000008.10:g.106573623C= , CM000670.1:g.106573623C=	GRCh37
NC_000008.9:g.106642799C=	NCBI36
NG_011723.1:g.247477C=
NG_011723.2:g.247477C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000407775.7:c.334C= MANE Select	ENSP00000384179.2:p.Arg112=
ENST00000407775.6:c.334C=	ENSP00000384179.2:p.Arg112=
ENST00000511341.6:n.1074C=
ENST00000517361.1:c.-63C=	ENSP00000428720.1:n.-63C=
ENST00000520027.5:c.-63C=	ENSP00000428149.1:n.-63C=
ENST00000520492.5:c.-63C=	ENSP00000430757.1:n.-63C=
ENST00000524235.5:n.547C=
NM_012082.3:c.334C=	NP_036214.2:p.Arg112=
XM_011516946.1:c.373C=	XP_011515248.1:p.Arg125=
XM_011516947.1:c.304C=	XP_011515249.1:p.Arg102=
XM_011516948.1:c.175C=	XP_011515250.1:p.Arg59=
XM_011516949.1:c.373C=	XP_011515251.1:p.Arg125=
NM_001362836.1:c.175C=	NP_001349765.1:p.Arg59=
NM_001362837.1:c.-63C=	NP_001349766.1:n.-63C=
XM_011516947.3:c.304C=	XP_011515249.1:p.Arg102=
NM_012082.4:c.334C= MANE Select	NP_036214.2:p.Arg112=
NM_001362836.2:c.175C=	NP_001349765.1:p.Arg59=
NM_001362837.2:c.-63C=	NP_001349766.1:n.-63C=