Canonical Allele Identifier: CA1149063902
Gene: HNRNPU HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.244864027_244864037delinsTCCTCCTCCTC , CM000663.2:g.244864027_244864037delinsTCCTCCTCCTC GRCh38
NC_000001.10:g.245027329_245027339delinsTCCTCCTCCTC , CM000663.1:g.245027329_245027339delinsTCCTCCTCCTC GRCh37
NC_000001.9:g.243093952_243093962delinsTCCTCCTCCTC NCBI36
NG_042184.1:g.5489_5499delinsGAGGAGGAGGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000283179.14:c.271_281delinsGAGGAGGAGGA ENSP00000283179.10:p.Glu91=
ENST00000444376.7:c.271_281delinsGAGGAGGAGGA ENSP00000393151.2:p.Glu91=
ENST00000476241.2:n.456_466delinsGAGGAGGAGGA
ENST00000638475.1:c.55_65delinsGAGGAGGAGGA ENSP00000491305.1:p.Glu19=
ENST00000638952.1:n.502_512delinsGAGGAGGAGGA
ENST00000640218.2:c.271_281delinsGAGGAGGAGGA MANE Select ENSP00000491215.1:p.Glu91=
ENST00000640306.1:c.271_281delinsGAGGAGGAGGA ENSP00000491685.1:p.Glu91=
ENST00000649899.1:n.495_505delinsGAGGAGGAGGA
ENST00000283179.13:c.271_281delinsGAGGAGGAGGA ENSP00000283179.9:p.Glu91=
ENST00000444376.6:c.271_281delinsGAGGAGGAGGA ENSP00000393151.2:p.Glu91=
ENST00000476241.1:n.455_465delinsGAGGAGGAGGA
NM_004501.3:c.271_281delinsGAGGAGGAGGA NP_004492.2:p.Glu91=
NM_031844.2:c.271_281delinsGAGGAGGAGGA NP_114032.2:p.Glu91=
NM_031844.3:c.271_281delinsGAGGAGGAGGA MANE Select NP_114032.2:p.Glu91=