Canonical Allele Identifier: CA1143949465

Gene: HNRNPU

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.244863852C= , CM000663.2:g.244863852C=	GRCh38
NC_000001.10:g.245027154C= , CM000663.1:g.245027154C=	GRCh37
NC_000001.9:g.243093777C=	NCBI36
NG_042184.1:g.5674G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000704074.1:c.134G=
ENST00000283179.14:c.456G=	ENSP00000283179.10:p.Ala152=
ENST00000444376.7:c.456G=	ENSP00000393151.2:p.Ala152=
ENST00000476241.2:n.641G=
ENST00000638475.1:c.240G=	ENSP00000491305.1:p.Ala80=
ENST00000638952.1:n.687G=
ENST00000640218.2:c.456G= MANE Select	ENSP00000491215.1:p.Ala152=
ENST00000640306.1:c.456G=	ENSP00000491685.1:p.Ala152=
ENST00000640440.1:c.156G=	ENSP00000491263.1:p.Ala52=
ENST00000649899.1:n.680G=
ENST00000283179.13:c.456G=	ENSP00000283179.9:p.Ala152=
ENST00000444376.6:c.456G=	ENSP00000393151.2:p.Ala152=
ENST00000476241.1:n.640G=
NM_004501.3:c.456G=	NP_004492.2:p.Ala152=
NM_031844.2:c.456G=	NP_114032.2:p.Ala152=
NM_031844.3:c.456G= MANE Select	NP_114032.2:p.Ala152=