Canonical Allele Identifier: CA1231007392
Gene: HNRNPU HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.244863699C= , CM000663.2:g.244863699C= GRCh38
NC_000001.10:g.245027001C= , CM000663.1:g.245027001C= GRCh37
NC_000001.9:g.243093624C= NCBI36
NG_042184.1:g.5827G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000704074.1:c.287G=
ENST00000283179.14:c.609G= ENSP00000283179.10:p.Ala203=
ENST00000444376.7:c.609G= ENSP00000393151.2:p.Ala203=
ENST00000476241.2:n.794G=
ENST00000638475.1:c.393G= ENSP00000491305.1:p.Ala131=
ENST00000638952.1:n.840G=
ENST00000640218.2:c.609G= MANE Select ENSP00000491215.1:p.Ala203=
ENST00000640306.1:c.609G= ENSP00000491685.1:p.Ala203=
ENST00000640440.1:c.309G= ENSP00000491263.1:p.Ala103=
ENST00000649899.1:n.833G=
ENST00000283179.13:c.609G= ENSP00000283179.9:p.Ala203=
ENST00000444376.6:c.609G= ENSP00000393151.2:p.Ala203=
ENST00000476241.1:n.793G=
NM_004501.3:c.609G= NP_004492.2:p.Ala203=
NM_031844.2:c.609G= NP_114032.2:p.Ala203=
NM_031844.3:c.609G= MANE Select NP_114032.2:p.Ala203=