Canonical Allele Identifier: CA1231007526
Gene: HNRNPU HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.244863958T= , CM000663.2:g.244863958T= GRCh38
NC_000001.10:g.245027260T= , CM000663.1:g.245027260T= GRCh37
NC_000001.9:g.243093883T= NCBI36
NG_042184.1:g.5568A=

Transcript Alleles

HGVS Amino-acid change
ENST00000704074.1:c.28A=
ENST00000283179.14:c.350A= ENSP00000283179.10:p.Asp117=
ENST00000444376.7:c.350A= ENSP00000393151.2:p.Asp117=
ENST00000476241.2:n.535A=
ENST00000638475.1:c.134A= ENSP00000491305.1:p.Asp45=
ENST00000638952.1:n.581A=
ENST00000640218.2:c.350A= MANE Select ENSP00000491215.1:p.Asp117=
ENST00000640306.1:c.350A= ENSP00000491685.1:p.Asp117=
ENST00000640440.1:c.50A= ENSP00000491263.1:p.Asp17=
ENST00000649899.1:n.574A=
ENST00000283179.13:c.350A= ENSP00000283179.9:p.Asp117=
ENST00000444376.6:c.350A= ENSP00000393151.2:p.Asp117=
ENST00000476241.1:n.534A=
NM_004501.3:c.350A= NP_004492.2:p.Asp117=
NM_031844.2:c.350A= NP_114032.2:p.Asp117=
NM_031844.3:c.350A= MANE Select NP_114032.2:p.Asp117=