Canonical Allele Identifier: CA1231007393
Gene: HNRNPU HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.244863700G= , CM000663.2:g.244863700G= GRCh38
NC_000001.10:g.245027002G= , CM000663.1:g.245027002G= GRCh37
NC_000001.9:g.243093625G= NCBI36
NG_042184.1:g.5826C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000704074.1:c.286C=
ENST00000283179.14:c.608C= ENSP00000283179.10:p.Ala203=
ENST00000444376.7:c.608C= ENSP00000393151.2:p.Ala203=
ENST00000476241.2:n.793C=
ENST00000638475.1:c.392C= ENSP00000491305.1:p.Ala131=
ENST00000638952.1:n.839C=
ENST00000640218.2:c.608C= MANE Select ENSP00000491215.1:p.Ala203=
ENST00000640306.1:c.608C= ENSP00000491685.1:p.Ala203=
ENST00000640440.1:c.308C= ENSP00000491263.1:p.Ala103=
ENST00000649899.1:n.832C=
ENST00000283179.13:c.608C= ENSP00000283179.9:p.Ala203=
ENST00000444376.6:c.608C= ENSP00000393151.2:p.Ala203=
ENST00000476241.1:n.792C=
NM_004501.3:c.608C= NP_004492.2:p.Ala203=
NM_031844.2:c.608C= NP_114032.2:p.Ala203=
NM_031844.3:c.608C= MANE Select NP_114032.2:p.Ala203=