Canonical Allele Identifier: CA1231007488

Gene: HNRNPU

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.244863876_244863879delinsCTCA , CM000663.2:g.244863876_244863879delinsCTCA	GRCh38
NC_000001.10:g.245027178_245027181delinsCTCA , CM000663.1:g.245027178_245027181delinsCTCA	GRCh37
NC_000001.9:g.243093801_243093804delinsCTCA	NCBI36
NG_042184.1:g.5647_5650delinsTGAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000704074.1:c.107_110delinsTGAG
ENST00000283179.14:c.429_432delinsTGAG	ENSP00000283179.10:p.Asp143=
ENST00000444376.7:c.429_432delinsTGAG	ENSP00000393151.2:p.Asp143=
ENST00000476241.2:n.614_617delinsTGAG
ENST00000638475.1:c.213_216delinsTGAG	ENSP00000491305.1:p.Asp71=
ENST00000638952.1:n.660_663delinsTGAG
ENST00000640218.2:c.429_432delinsTGAG MANE Select	ENSP00000491215.1:p.Asp143=
ENST00000640306.1:c.429_432delinsTGAG	ENSP00000491685.1:p.Asp143=
ENST00000640440.1:c.129_132delinsTGAG	ENSP00000491263.1:p.Asp43=
ENST00000649899.1:n.653_656delinsTGAG
ENST00000283179.13:c.429_432delinsTGAG	ENSP00000283179.9:p.Asp143=
ENST00000444376.6:c.429_432delinsTGAG	ENSP00000393151.2:p.Asp143=
ENST00000476241.1:n.613_616delinsTGAG
NM_004501.3:c.429_432delinsTGAG	NP_004492.2:p.Asp143=
NM_031844.2:c.429_432delinsTGAG	NP_114032.2:p.Asp143=
NM_031844.3:c.429_432delinsTGAG MANE Select	NP_114032.2:p.Asp143=