Canonical Allele Identifier: CA2586968605

Gene: HNRNPU

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.244863977dup , CM000663.2:g.244863977dup	GRCh38
NC_000001.10:g.245027279dup , CM000663.1:g.245027279dup	GRCh37
NC_000001.9:g.243093902dup	NCBI36
NG_042184.1:g.5552dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000704074.1:c.12dup
ENST00000283179.14:c.334dup	ENSP00000283179.10:p.Ala112GlyfsTer?
ENST00000444376.7:c.334dup	ENSP00000393151.2:p.Ala112GlyfsTer?
ENST00000476241.2:n.519dup
ENST00000638475.1:c.118dup	ENSP00000491305.1:p.Ala40GlyfsTer?
ENST00000638952.1:n.565dup
ENST00000640218.2:c.334dup MANE Select	ENSP00000491215.1:p.Ala112GlyfsTer?
ENST00000640306.1:c.334dup	ENSP00000491685.1:p.Ala112GlyfsTer?
ENST00000640440.1:c.34dup	ENSP00000491263.1:p.Ala12GlyfsTer?
ENST00000649899.1:n.558dup
ENST00000283179.13:c.334dup	ENSP00000283179.9:p.Ala112GlyfsTer?
ENST00000444376.6:c.334dup	ENSP00000393151.2:p.Ala112GlyfsTer?
ENST00000476241.1:n.518dup
NM_004501.3:c.334dup	NP_004492.2:p.Ala112GlyfsTer?
NM_031844.2:c.334dup	NP_114032.2:p.Ala112GlyfsTer?
NM_031844.3:c.334dup MANE Select	NP_114032.2:p.Ala112GlyfsTer?