Canonical Allele Identifier: CA1231007470

Gene: HNRNPU

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.244863835T= , CM000663.2:g.244863835T=	GRCh38
NC_000001.10:g.245027137T= , CM000663.1:g.245027137T=	GRCh37
NC_000001.9:g.243093760T=	NCBI36
NG_042184.1:g.5691A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000704074.1:c.151A=
ENST00000283179.14:c.473A=	ENSP00000283179.10:p.His158=
ENST00000444376.7:c.473A=	ENSP00000393151.2:p.His158=
ENST00000476241.2:n.658A=
ENST00000638475.1:c.257A=	ENSP00000491305.1:p.His86=
ENST00000638952.1:n.704A=
ENST00000640218.2:c.473A= MANE Select	ENSP00000491215.1:p.His158=
ENST00000640306.1:c.473A=	ENSP00000491685.1:p.His158=
ENST00000640440.1:c.173A=	ENSP00000491263.1:p.His58=
ENST00000649899.1:n.697A=
ENST00000283179.13:c.473A=	ENSP00000283179.9:p.His158=
ENST00000444376.6:c.473A=	ENSP00000393151.2:p.His158=
ENST00000476241.1:n.657A=
NM_004501.3:c.473A=	NP_004492.2:p.His158=
NM_031844.2:c.473A=	NP_114032.2:p.His158=
NM_031844.3:c.473A= MANE Select	NP_114032.2:p.His158=