Canonical Allele Identifier: CA1231007498

Gene: HNRNPU

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.244863905_244863907delinsCGT , CM000663.2:g.244863905_244863907delinsCGT	GRCh38
NC_000001.10:g.245027207_245027209delinsCGT , CM000663.1:g.245027207_245027209delinsCGT	GRCh37
NC_000001.9:g.243093830_243093832delinsCGT	NCBI36
NG_042184.1:g.5619_5621delinsACG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000704074.1:c.79_81delinsACG
ENST00000283179.14:c.401_403delinsACG	ENSP00000283179.10:p.Asp134=
ENST00000444376.7:c.401_403delinsACG	ENSP00000393151.2:p.Asp134=
ENST00000476241.2:n.586_588delinsACG
ENST00000638475.1:c.185_187delinsACG	ENSP00000491305.1:p.Asp62=
ENST00000638952.1:n.632_634delinsACG
ENST00000640218.2:c.401_403delinsACG MANE Select	ENSP00000491215.1:p.Asp134=
ENST00000640306.1:c.401_403delinsACG	ENSP00000491685.1:p.Asp134=
ENST00000640440.1:c.101_103delinsACG	ENSP00000491263.1:p.Asp34=
ENST00000649899.1:n.625_627delinsACG
ENST00000283179.13:c.401_403delinsACG	ENSP00000283179.9:p.Asp134=
ENST00000444376.6:c.401_403delinsACG	ENSP00000393151.2:p.Asp134=
ENST00000476241.1:n.585_587delinsACG
NM_004501.3:c.401_403delinsACG	NP_004492.2:p.Asp134=
NM_031844.2:c.401_403delinsACG	NP_114032.2:p.Asp134=
NM_031844.3:c.401_403delinsACG MANE Select	NP_114032.2:p.Asp134=