Canonical Allele Identifier: CA1231007452

Gene: HNRNPU

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.244863804C= , CM000663.2:g.244863804C=	GRCh38
NC_000001.10:g.245027106C= , CM000663.1:g.245027106C=	GRCh37
NC_000001.9:g.243093729C=	NCBI36
NG_042184.1:g.5722G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000704074.1:c.182G=
ENST00000283179.14:c.504G=	ENSP00000283179.10:p.Thr168=
ENST00000444376.7:c.504G=	ENSP00000393151.2:p.Thr168=
ENST00000476241.2:n.689G=
ENST00000638475.1:c.288G=	ENSP00000491305.1:p.Thr96=
ENST00000638952.1:n.735G=
ENST00000640218.2:c.504G= MANE Select	ENSP00000491215.1:p.Thr168=
ENST00000640306.1:c.504G=	ENSP00000491685.1:p.Thr168=
ENST00000640440.1:c.204G=	ENSP00000491263.1:p.Thr68=
ENST00000649899.1:n.728G=
ENST00000283179.13:c.504G=	ENSP00000283179.9:p.Thr168=
ENST00000444376.6:c.504G=	ENSP00000393151.2:p.Thr168=
ENST00000476241.1:n.688G=
NM_004501.3:c.504G=	NP_004492.2:p.Thr168=
NM_031844.2:c.504G=	NP_114032.2:p.Thr168=
NM_031844.3:c.504G= MANE Select	NP_114032.2:p.Thr168=