Canonical Allele Identifier: CA1231007567

Gene: HNRNPU

Linked Data

• dbSNP Id: rs1680932556

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.244864047_244864058del , CM000663.2:g.244864047_244864058del	GRCh38
NC_000001.10:g.245027349_245027360del , CM000663.1:g.245027349_245027360del	GRCh37
NC_000001.9:g.243093972_243093983del	NCBI36
NG_042184.1:g.5476_5487del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000283179.14:c.258_269del	ENSP00000283179.10:p.Glu87_Glu90del
ENST00000444376.7:c.258_269del	ENSP00000393151.2:p.Glu87_Glu90del
ENST00000476241.2:n.443_454del
ENST00000638475.1:c.42_53del	ENSP00000491305.1:p.Glu15_Glu18del
ENST00000638952.1:n.489_500del
ENST00000640218.2:c.258_269del MANE Select	ENSP00000491215.1:p.Glu87_Glu90del
ENST00000640306.1:c.258_269del	ENSP00000491685.1:p.Glu87_Glu90del
ENST00000649899.1:n.482_493del
ENST00000283179.13:c.258_269del	ENSP00000283179.9:p.Glu87_Glu90del
ENST00000444376.6:c.258_269del	ENSP00000393151.2:p.Glu87_Glu90del
ENST00000476241.1:n.442_453del
NM_004501.3:c.258_269del	NP_004492.2:p.Glu87_Glu90del
NM_031844.2:c.258_269del	NP_114032.2:p.Glu87_Glu90del
NM_031844.3:c.258_269del MANE Select	NP_114032.2:p.Glu87_Glu90del