Canonical Allele Identifier: CA1231007447

Gene: HNRNPU

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.244863795_244863825delinsTTGCTGCTGCGTCGCCGGCGGTTGAGGCTGC , CM000663.2:g.244863795_244863825delinsTTGCTGCTGCGTCGCCGGCGGTTGAGGCTGC	GRCh38
NC_000001.10:g.245027097_245027127delinsTTGCTGCTGCGTCGCCGGCGGTTGAGGCTGC , CM000663.1:g.245027097_245027127delinsTTGCTGCTGCGTCGCCGGCGGTTGAGGCTGC	GRCh37
NC_000001.9:g.243093720_243093750delinsTTGCTGCTGCGTCGCCGGCGGTTGAGGCTGC	NCBI36
NG_042184.1:g.5701_5731delinsGCAGCCTCAACCGCCGGCGACGCAGCAGCAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000704074.1:c.161_191delinsGCAGCCTCAACCGCCGGCGACGCAGCAGCAA
ENST00000283179.14:c.483_513delinsGCAGCCTCAACCGCCGGCGACGCAGCAGCAA	ENSP00000283179.10:p.Gln161=
ENST00000444376.7:c.483_513delinsGCAGCCTCAACCGCCGGCGACGCAGCAGCAA	ENSP00000393151.2:p.Gln161=
ENST00000476241.2:n.668_698delinsGCAGCCTCAACCGCCGGCGACGCAGCAGCAA
ENST00000638475.1:c.267_297delinsGCAGCCTCAACCGCCGGCGACGCAGCAGCAA	ENSP00000491305.1:p.Gln89=
ENST00000638952.1:n.714_744delinsGCAGCCTCAACCGCCGGCGACGCAGCAGCAA
ENST00000640218.2:c.483_513delinsGCAGCCTCAACCGCCGGCGACGCAGCAGCAA MANE Select	ENSP00000491215.1:p.Gln161=
ENST00000640306.1:c.483_513delinsGCAGCCTCAACCGCCGGCGACGCAGCAGCAA	ENSP00000491685.1:p.Gln161=
ENST00000640440.1:c.183_213delinsGCAGCCTCAACCGCCGGCGACGCAGCAGCAA	ENSP00000491263.1:p.Gln61=
ENST00000649899.1:n.707_737delinsGCAGCCTCAACCGCCGGCGACGCAGCAGCAA
ENST00000283179.13:c.483_513delinsGCAGCCTCAACCGCCGGCGACGCAGCAGCAA	ENSP00000283179.9:p.Gln161=
ENST00000444376.6:c.483_513delinsGCAGCCTCAACCGCCGGCGACGCAGCAGCAA	ENSP00000393151.2:p.Gln161=
ENST00000476241.1:n.667_697delinsGCAGCCTCAACCGCCGGCGACGCAGCAGCAA
NM_004501.3:c.483_513delinsGCAGCCTCAACCGCCGGCGACGCAGCAGCAA	NP_004492.2:p.Gln161=
NM_031844.2:c.483_513delinsGCAGCCTCAACCGCCGGCGACGCAGCAGCAA	NP_114032.2:p.Gln161=
NM_031844.3:c.483_513delinsGCAGCCTCAACCGCCGGCGACGCAGCAGCAA MANE Select	NP_114032.2:p.Gln161=