Canonical Allele Identifier: CA1231007507

Gene: HNRNPU

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.244863920C= , CM000663.2:g.244863920C=	GRCh38
NC_000001.10:g.245027222C= , CM000663.1:g.245027222C=	GRCh37
NC_000001.9:g.243093845C=	NCBI36
NG_042184.1:g.5606G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000704074.1:c.66G=
ENST00000283179.14:c.388G=	ENSP00000283179.10:p.Asp130=
ENST00000444376.7:c.388G=	ENSP00000393151.2:p.Asp130=
ENST00000476241.2:n.573G=
ENST00000638475.1:c.172G=	ENSP00000491305.1:p.Asp58=
ENST00000638952.1:n.619G=
ENST00000640218.2:c.388G= MANE Select	ENSP00000491215.1:p.Asp130=
ENST00000640306.1:c.388G=	ENSP00000491685.1:p.Asp130=
ENST00000640440.1:c.88G=	ENSP00000491263.1:p.Asp30=
ENST00000649899.1:n.612G=
ENST00000283179.13:c.388G=	ENSP00000283179.9:p.Asp130=
ENST00000444376.6:c.388G=	ENSP00000393151.2:p.Asp130=
ENST00000476241.1:n.572G=
NM_004501.3:c.388G=	NP_004492.2:p.Asp130=
NM_031844.2:c.388G=	NP_114032.2:p.Asp130=
NM_031844.3:c.388G= MANE Select	NP_114032.2:p.Asp130=