Canonical Allele Identifier: CA1231007570

Gene: HNRNPU

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.244864042_244864047delinsTCTTCC , CM000663.2:g.244864042_244864047delinsTCTTCC	GRCh38
NC_000001.10:g.245027344_245027349delinsTCTTCC , CM000663.1:g.245027344_245027349delinsTCTTCC	GRCh37
NC_000001.9:g.243093967_243093972delinsTCTTCC	NCBI36
NG_042184.1:g.5479_5484delinsGGAAGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000283179.14:c.261_266delinsGGAAGA	ENSP00000283179.10:p.Glu87=
ENST00000444376.7:c.261_266delinsGGAAGA	ENSP00000393151.2:p.Glu87=
ENST00000476241.2:n.446_451delinsGGAAGA
ENST00000638475.1:c.45_50delinsGGAAGA	ENSP00000491305.1:p.Glu15=
ENST00000638952.1:n.492_497delinsGGAAGA
ENST00000640218.2:c.261_266delinsGGAAGA MANE Select	ENSP00000491215.1:p.Glu87=
ENST00000640306.1:c.261_266delinsGGAAGA	ENSP00000491685.1:p.Glu87=
ENST00000649899.1:n.485_490delinsGGAAGA
ENST00000283179.13:c.261_266delinsGGAAGA	ENSP00000283179.9:p.Glu87=
ENST00000444376.6:c.261_266delinsGGAAGA	ENSP00000393151.2:p.Glu87=
ENST00000476241.1:n.445_450delinsGGAAGA
NM_004501.3:c.261_266delinsGGAAGA	NP_004492.2:p.Glu87=
NM_031844.2:c.261_266delinsGGAAGA	NP_114032.2:p.Glu87=
NM_031844.3:c.261_266delinsGGAAGA MANE Select	NP_114032.2:p.Glu87=