Canonical Allele Identifier: CA2651343582

Gene: HNRNPU

Linked Data

• gnomAD v4: 1-244863980-TCTC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.244863984_244863986del , CM000663.2:g.244863984_244863986del	GRCh38
NC_000001.10:g.245027286_245027288del , CM000663.1:g.245027286_245027288del	GRCh37
NC_000001.9:g.243093909_243093911del	NCBI36
NG_042184.1:g.5543_5545del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000283179.14:c.325_327del	ENSP00000283179.10:p.Glu109del
ENST00000444376.7:c.325_327del	ENSP00000393151.2:p.Glu109del
ENST00000476241.2:n.510_512del
ENST00000638475.1:c.109_111del	ENSP00000491305.1:p.Glu37del
ENST00000638952.1:n.556_558del
ENST00000640218.2:c.325_327del MANE Select	ENSP00000491215.1:p.Glu109del
ENST00000640306.1:c.325_327del	ENSP00000491685.1:p.Glu109del
ENST00000640440.1:c.25_27del	ENSP00000491263.1:p.Glu9del
ENST00000649899.1:n.549_551del
ENST00000283179.13:c.325_327del	ENSP00000283179.9:p.Glu109del
ENST00000444376.6:c.325_327del	ENSP00000393151.2:p.Glu109del
ENST00000476241.1:n.509_511del
NM_004501.3:c.325_327del	NP_004492.2:p.Glu109del
NM_031844.2:c.325_327del	NP_114032.2:p.Glu109del
NM_031844.3:c.325_327del MANE Select	NP_114032.2:p.Glu109del