Canonical Allele Identifier: CA1808332098

Gene: ZFPM2 ZFPM2-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.105801833T= , CM000670.2:g.105801833T=	GRCh38
NC_000008.10:g.106814061T= , CM000670.1:g.106814061T=	GRCh37
NC_000008.9:g.106883237T=	NCBI36
NG_011723.1:g.487915T=
NG_011723.2:g.487915T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000407775.7:c.1751T= (ZFPM2) MANE Select	ENSP00000384179.2:p.Phe584=
ENST00000407775.6:c.1751T= (ZFPM2)	ENSP00000384179.2:p.Phe584=
ENST00000517361.1:c.1355T= (ZFPM2)	ENSP00000428720.1:p.Phe452=
ENST00000520492.5:c.1355T= (ZFPM2)	ENSP00000430757.1:p.Phe452=
ENST00000522296.1:n.1545T= (ZFPM2)
NM_012082.3:c.1751T= (ZFPM2)	NP_036214.2:p.Phe584=
NR_125796.1:n.180-3391A= (ZFPM2-AS1)
NR_125797.1:n.191-3391A= (ZFPM2-AS1)
XM_011516946.1:c.1790T= (ZFPM2)	XP_011515248.1:p.Phe597=
XM_011516947.1:c.1721T= (ZFPM2)	XP_011515249.1:p.Phe574=
XM_011516948.1:c.1592T= (ZFPM2)	XP_011515250.1:p.Phe531=
XM_011516949.1:c.1583T= (ZFPM2)	XP_011515251.1:p.Phe528=
NM_001362836.1:c.1592T= (ZFPM2)	NP_001349765.1:p.Phe531=
NM_001362837.1:c.1355T= (ZFPM2)	NP_001349766.1:p.Phe452=
XM_011516947.3:c.1721T= (ZFPM2)	XP_011515249.1:p.Phe574=
NM_012082.4:c.1751T= (ZFPM2) MANE Select	NP_036214.2:p.Phe584=
NM_001362836.2:c.1592T= (ZFPM2)	NP_001349765.1:p.Phe531=
NM_001362837.2:c.1355T= (ZFPM2)	NP_001349766.1:p.Phe452=