Canonical Allele Identifier: CA1231007455

Gene: HNRNPU

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.244863811G= , CM000663.2:g.244863811G=	GRCh38
NC_000001.10:g.245027113G= , CM000663.1:g.245027113G=	GRCh37
NC_000001.9:g.243093736G=	NCBI36
NG_042184.1:g.5715C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000704074.1:c.175C=
ENST00000283179.14:c.497C=	ENSP00000283179.10:p.Pro166=
ENST00000444376.7:c.497C=	ENSP00000393151.2:p.Pro166=
ENST00000476241.2:n.682C=
ENST00000638475.1:c.281C=	ENSP00000491305.1:p.Pro94=
ENST00000638952.1:n.728C=
ENST00000640218.2:c.497C= MANE Select	ENSP00000491215.1:p.Pro166=
ENST00000640306.1:c.497C=	ENSP00000491685.1:p.Pro166=
ENST00000640440.1:c.197C=	ENSP00000491263.1:p.Pro66=
ENST00000649899.1:n.721C=
ENST00000283179.13:c.497C=	ENSP00000283179.9:p.Pro166=
ENST00000444376.6:c.497C=	ENSP00000393151.2:p.Pro166=
ENST00000476241.1:n.681C=
NM_004501.3:c.497C=	NP_004492.2:p.Pro166=
NM_031844.2:c.497C=	NP_114032.2:p.Pro166=
NM_031844.3:c.497C= MANE Select	NP_114032.2:p.Pro166=