Canonical Allele Identifier: CA1147345275

Gene: HNRNPU

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.244863665T= , CM000663.2:g.244863665T=	GRCh38
NC_000001.10:g.245026967T= , CM000663.1:g.245026967T=	GRCh37
NC_000001.9:g.243093590T=	NCBI36
NG_042184.1:g.5861A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000704074.1:c.312+9A=
ENST00000283179.14:c.634+9A=	ENSP00000283179.10:n.634+9A=
ENST00000444376.7:c.634+9A=	ENSP00000393151.2:n.634+9A=
ENST00000476241.2:n.819+9A=
ENST00000638475.1:c.418+9A=	ENSP00000491305.1:n.418+9A=
ENST00000638952.1:n.874A=
ENST00000640218.2:c.643A= MANE Select	ENSP00000491215.1:p.Lys215=
ENST00000640306.1:c.634+9A=	ENSP00000491685.1:n.634+9A=
ENST00000640440.1:c.334+9A=	ENSP00000491263.1:n.334+9A=
ENST00000649899.1:n.858+9A=
ENST00000283179.13:c.643A=	ENSP00000283179.9:p.Lys215=
ENST00000444376.6:c.634+9A=	ENSP00000393151.2:n.634+9A=
ENST00000476241.1:n.818+9A=
NM_004501.3:c.634+9A=	NP_004492.2:n.634+9A=
NM_031844.2:c.643A=	NP_114032.2:p.Lys215=
NM_031844.3:c.643A= MANE Select	NP_114032.2:p.Lys215=