Canonical Allele Identifier: CA1231007489

Gene: HNRNPU

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.244863882T= , CM000663.2:g.244863882T=	GRCh38
NC_000001.10:g.245027184T= , CM000663.1:g.245027184T=	GRCh37
NC_000001.9:g.243093807T=	NCBI36
NG_042184.1:g.5644A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000704074.1:c.104A=
ENST00000283179.14:c.426A=	ENSP00000283179.10:p.Glu142=
ENST00000444376.7:c.426A=	ENSP00000393151.2:p.Glu142=
ENST00000476241.2:n.611A=
ENST00000638475.1:c.210A=	ENSP00000491305.1:p.Glu70=
ENST00000638952.1:n.657A=
ENST00000640218.2:c.426A= MANE Select	ENSP00000491215.1:p.Glu142=
ENST00000640306.1:c.426A=	ENSP00000491685.1:p.Glu142=
ENST00000640440.1:c.126A=	ENSP00000491263.1:p.Glu42=
ENST00000649899.1:n.650A=
ENST00000283179.13:c.426A=	ENSP00000283179.9:p.Glu142=
ENST00000444376.6:c.426A=	ENSP00000393151.2:p.Glu142=
ENST00000476241.1:n.610A=
NM_004501.3:c.426A=	NP_004492.2:p.Glu142=
NM_031844.2:c.426A=	NP_114032.2:p.Glu142=
NM_031844.3:c.426A= MANE Select	NP_114032.2:p.Glu142=