Canonical Allele Identifier: CA1231007537
Gene: HNRNPU HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.244863985_244863992delinsTCTCCTAG , CM000663.2:g.244863985_244863992delinsTCTCCTAG GRCh38
NC_000001.10:g.245027287_245027294delinsTCTCCTAG , CM000663.1:g.245027287_245027294delinsTCTCCTAG GRCh37
NC_000001.9:g.243093910_243093917delinsTCTCCTAG NCBI36
NG_042184.1:g.5534_5541delinsCTAGGAGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000283179.14:c.316_323delinsCTAGGAGA ENSP00000283179.10:p.Leu106=
ENST00000444376.7:c.316_323delinsCTAGGAGA ENSP00000393151.2:p.Leu106=
ENST00000476241.2:n.501_508delinsCTAGGAGA
ENST00000638475.1:c.100_107delinsCTAGGAGA ENSP00000491305.1:p.Leu34=
ENST00000638952.1:n.547_554delinsCTAGGAGA
ENST00000640218.2:c.316_323delinsCTAGGAGA MANE Select ENSP00000491215.1:p.Leu106=
ENST00000640306.1:c.316_323delinsCTAGGAGA ENSP00000491685.1:p.Leu106=
ENST00000640440.1:c.16_23delinsCTAGGAGA ENSP00000491263.1:p.Leu6=
ENST00000649899.1:n.540_547delinsCTAGGAGA
ENST00000283179.13:c.316_323delinsCTAGGAGA ENSP00000283179.9:p.Leu106=
ENST00000444376.6:c.316_323delinsCTAGGAGA ENSP00000393151.2:p.Leu106=
ENST00000476241.1:n.500_507delinsCTAGGAGA
NM_004501.3:c.316_323delinsCTAGGAGA NP_004492.2:p.Leu106=
NM_031844.2:c.316_323delinsCTAGGAGA NP_114032.2:p.Leu106=
NM_031844.3:c.316_323delinsCTAGGAGA MANE Select NP_114032.2:p.Leu106=