Canonical Allele Identifier: CA1143373646

Gene: HNRNPU

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.244863934T= , CM000663.2:g.244863934T=	GRCh38
NC_000001.10:g.245027236T= , CM000663.1:g.245027236T=	GRCh37
NC_000001.9:g.243093859T=	NCBI36
NG_042184.1:g.5592A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000704074.1:c.52A=
ENST00000283179.14:c.374A=	ENSP00000283179.10:p.Glu125=
ENST00000444376.7:c.374A=	ENSP00000393151.2:p.Glu125=
ENST00000476241.2:n.559A=
ENST00000638475.1:c.158A=	ENSP00000491305.1:p.Glu53=
ENST00000638952.1:n.605A=
ENST00000640218.2:c.374A= MANE Select	ENSP00000491215.1:p.Glu125=
ENST00000640306.1:c.374A=	ENSP00000491685.1:p.Glu125=
ENST00000640440.1:c.74A=	ENSP00000491263.1:p.Glu25=
ENST00000649899.1:n.598A=
ENST00000283179.13:c.374A=	ENSP00000283179.9:p.Glu125=
ENST00000444376.6:c.374A=	ENSP00000393151.2:p.Glu125=
ENST00000476241.1:n.558A=
NM_004501.3:c.374A=	NP_004492.2:p.Glu125=
NM_031844.2:c.374A=	NP_114032.2:p.Glu125=
NM_031844.3:c.374A= MANE Select	NP_114032.2:p.Glu125=