Canonical Allele Identifier: CA2748454211

Gene: HNRNPU

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.244863858_244863860dup , CM000663.2:g.244863858_244863860dup	GRCh38
NC_000001.10:g.245027160_245027162dup , CM000663.1:g.245027160_245027162dup	GRCh37
NC_000001.9:g.243093783_243093785dup	NCBI36
NG_042184.1:g.5667_5669dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000704074.1:c.127_129dup
ENST00000283179.14:c.449_451dup	ENSP00000283179.10:p.Glu150_Gly151insGlu
ENST00000444376.7:c.449_451dup	ENSP00000393151.2:p.Glu150_Gly151insGlu
ENST00000476241.2:n.634_636dup
ENST00000638475.1:c.233_235dup	ENSP00000491305.1:p.Glu78_Gly79insGlu
ENST00000638952.1:n.680_682dup
ENST00000640218.2:c.449_451dup MANE Select	ENSP00000491215.1:p.Glu150_Gly151insGlu
ENST00000640306.1:c.449_451dup	ENSP00000491685.1:p.Glu150_Gly151insGlu
ENST00000640440.1:c.149_151dup	ENSP00000491263.1:p.Glu50_Gly51insGlu
ENST00000649899.1:n.673_675dup
ENST00000283179.13:c.449_451dup	ENSP00000283179.9:p.Glu150_Gly151insGlu
ENST00000444376.6:c.449_451dup	ENSP00000393151.2:p.Glu150_Gly151insGlu
ENST00000476241.1:n.633_635dup
NM_004501.3:c.449_451dup	NP_004492.2:p.Glu150_Gly151insGlu
NM_031844.2:c.449_451dup	NP_114032.2:p.Glu150_Gly151insGlu
NM_031844.3:c.449_451dup MANE Select	NP_114032.2:p.Glu150_Gly151insGlu