Canonical Allele Identifier: CA1231007568

Gene: HNRNPU

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.244864039_244864040delinsTC , CM000663.2:g.244864039_244864040delinsTC	GRCh38
NC_000001.10:g.245027341_245027342delinsTC , CM000663.1:g.245027341_245027342delinsTC	GRCh37
NC_000001.9:g.243093964_243093965delinsTC	NCBI36
NG_042184.1:g.5486_5487delinsGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000283179.14:c.268_269delinsGA	ENSP00000283179.10:p.Glu90=
ENST00000444376.7:c.268_269delinsGA	ENSP00000393151.2:p.Glu90=
ENST00000476241.2:n.453_454delinsGA
ENST00000638475.1:c.52_53delinsGA	ENSP00000491305.1:p.Glu18=
ENST00000638952.1:n.499_500delinsGA
ENST00000640218.2:c.268_269delinsGA MANE Select	ENSP00000491215.1:p.Glu90=
ENST00000640306.1:c.268_269delinsGA	ENSP00000491685.1:p.Glu90=
ENST00000649899.1:n.492_493delinsGA
ENST00000283179.13:c.268_269delinsGA	ENSP00000283179.9:p.Glu90=
ENST00000444376.6:c.268_269delinsGA	ENSP00000393151.2:p.Glu90=
ENST00000476241.1:n.452_453delinsGA
NM_004501.3:c.268_269delinsGA	NP_004492.2:p.Glu90=
NM_031844.2:c.268_269delinsGA	NP_114032.2:p.Glu90=
NM_031844.3:c.268_269delinsGA MANE Select	NP_114032.2:p.Glu90=