Canonical Allele Identifier: CA2526161833

Gene: HNRNPU

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.244863649_244863657dup , CM000663.2:g.244863649_244863657dup	GRCh38
NC_000001.10:g.245026951_245026959dup , CM000663.1:g.245026951_245026959dup	GRCh37
NC_000001.9:g.243093574_243093582dup	NCBI36
NG_042184.1:g.5878_5886dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000704074.1:c.312+26_312+34dup
ENST00000283179.14:c.634+26_634+34dup	ENSP00000283179.10:n.634+26_634+34dup
ENST00000444376.7:c.634+26_634+34dup	ENSP00000393151.2:n.634+26_634+34dup
ENST00000476241.2:n.819+26_819+34dup
ENST00000638475.1:c.418+26_418+34dup	ENSP00000491305.1:n.418+26_418+34dup
ENST00000638952.1:n.891_899dup
ENST00000640218.2:c.660_668dup MANE Select	ENSP00000491215.1:p.Gly223_Arg224insGlyGlyGly
ENST00000640306.1:c.634+26_634+34dup	ENSP00000491685.1:n.634+26_634+34dup
ENST00000640440.1:c.334+26_334+34dup	ENSP00000491263.1:n.334+26_334+34dup
ENST00000649899.1:n.858+26_858+34dup
ENST00000283179.13:c.660_668dup	ENSP00000283179.9:p.Gly223_Arg224insGlyGlyGly
ENST00000444376.6:c.634+26_634+34dup	ENSP00000393151.2:n.634+26_634+34dup
ENST00000476241.1:n.818+26_818+34dup
NM_004501.3:c.634+26_634+34dup	NP_004492.2:n.634+26_634+34dup
NM_031844.2:c.660_668dup	NP_114032.2:p.Gly223_Arg224insGlyGlyGly
NM_031844.3:c.660_668dup MANE Select	NP_114032.2:p.Gly223_Arg224insGlyGlyGly