Canonical Allele Identifier: CA1231007566
Gene: HNRNPU HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.244864038_244864050delinsTTCCTCTTCCTCC , CM000663.2:g.244864038_244864050delinsTTCCTCTTCCTCC GRCh38
NC_000001.10:g.245027340_245027352delinsTTCCTCTTCCTCC , CM000663.1:g.245027340_245027352delinsTTCCTCTTCCTCC GRCh37
NC_000001.9:g.243093963_243093975delinsTTCCTCTTCCTCC NCBI36
NG_042184.1:g.5476_5488delinsGGAGGAAGAGGAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000283179.14:c.258_270delinsGGAGGAAGAGGAA ENSP00000283179.10:p.Glu86=
ENST00000444376.7:c.258_270delinsGGAGGAAGAGGAA ENSP00000393151.2:p.Glu86=
ENST00000476241.2:n.443_455delinsGGAGGAAGAGGAA
ENST00000638475.1:c.42_54delinsGGAGGAAGAGGAA ENSP00000491305.1:p.Glu14=
ENST00000638952.1:n.489_501delinsGGAGGAAGAGGAA
ENST00000640218.2:c.258_270delinsGGAGGAAGAGGAA MANE Select ENSP00000491215.1:p.Glu86=
ENST00000640306.1:c.258_270delinsGGAGGAAGAGGAA ENSP00000491685.1:p.Glu86=
ENST00000649899.1:n.482_494delinsGGAGGAAGAGGAA
ENST00000283179.13:c.258_270delinsGGAGGAAGAGGAA ENSP00000283179.9:p.Glu86=
ENST00000444376.6:c.258_270delinsGGAGGAAGAGGAA ENSP00000393151.2:p.Glu86=
ENST00000476241.1:n.442_454delinsGGAGGAAGAGGAA
NM_004501.3:c.258_270delinsGGAGGAAGAGGAA NP_004492.2:p.Glu86=
NM_031844.2:c.258_270delinsGGAGGAAGAGGAA NP_114032.2:p.Glu86=
NM_031844.3:c.258_270delinsGGAGGAAGAGGAA MANE Select NP_114032.2:p.Glu86=