Canonical Allele Identifier: CA2017997758
Gene: HNRNPU HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.244863751_244863764del , CM000663.2:g.244863751_244863764del GRCh38
NC_000001.10:g.245027053_245027066del , CM000663.1:g.245027053_245027066del GRCh37
NC_000001.9:g.243093676_243093689del NCBI36
NG_042184.1:g.5765_5778del

Transcript Alleles

HGVS Amino-acid Change
ENST00000704074.1:c.225_238del
ENST00000283179.14:c.547_560del ENSP00000283179.10:p.Ala183GlnfsTer26
ENST00000444376.7:c.547_560del ENSP00000393151.2:p.Ala183GlnfsTer?
ENST00000476241.2:n.732_745del
ENST00000638475.1:c.331_344del ENSP00000491305.1:p.Ala111GlnfsTer?
ENST00000638952.1:n.778_791del
ENST00000640218.2:c.547_560del MANE Select ENSP00000491215.1:p.Ala183GlnfsTer26
ENST00000640306.1:c.547_560del ENSP00000491685.1:p.Ala183GlnfsTer?
ENST00000640440.1:c.247_260del ENSP00000491263.1:p.Ala83GlnfsTer?
ENST00000649899.1:n.771_784del
ENST00000283179.13:c.547_560del ENSP00000283179.9:p.Ala183GlnfsTer26
ENST00000444376.6:c.547_560del ENSP00000393151.2:p.Ala183GlnfsTer?
ENST00000476241.1:n.731_744del
NM_004501.3:c.547_560del NP_004492.2:p.Ala183GlnfsTer?
NM_031844.2:c.547_560del NP_114032.2:p.Ala183GlnfsTer26
NM_031844.3:c.547_560del MANE Select NP_114032.2:p.Ala183GlnfsTer26