Canonical Allele Identifier: CA1146316102
Gene: HNRNPU HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.244863956A= , CM000663.2:g.244863956A= GRCh38
NC_000001.10:g.245027258A= , CM000663.1:g.245027258A= GRCh37
NC_000001.9:g.243093881A= NCBI36
NG_042184.1:g.5570T=

Transcript Alleles

HGVS Amino-acid change
ENST00000704074.1:c.30T=
ENST00000283179.14:c.352T= ENSP00000283179.10:p.Ser118=
ENST00000444376.7:c.352T= ENSP00000393151.2:p.Ser118=
ENST00000476241.2:n.537T=
ENST00000638475.1:c.136T= ENSP00000491305.1:p.Ser46=
ENST00000638952.1:n.583T=
ENST00000640218.2:c.352T= MANE Select ENSP00000491215.1:p.Ser118=
ENST00000640306.1:c.352T= ENSP00000491685.1:p.Ser118=
ENST00000640440.1:c.52T= ENSP00000491263.1:p.Ser18=
ENST00000649899.1:n.576T=
ENST00000283179.13:c.352T= ENSP00000283179.9:p.Ser118=
ENST00000444376.6:c.352T= ENSP00000393151.2:p.Ser118=
ENST00000476241.1:n.536T=
NM_004501.3:c.352T= NP_004492.2:p.Ser118=
NM_031844.2:c.352T= NP_114032.2:p.Ser118=
NM_031844.3:c.352T= MANE Select NP_114032.2:p.Ser118=