Canonical Allele Identifier: CA1231007385

Gene: HNRNPU

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.244863689_244863692delinsGGCC , CM000663.2:g.244863689_244863692delinsGGCC	GRCh38
NC_000001.10:g.245026991_245026994delinsGGCC , CM000663.1:g.245026991_245026994delinsGGCC	GRCh37
NC_000001.9:g.243093614_243093617delinsGGCC	NCBI36
NG_042184.1:g.5834_5837delinsGGCC

Transcript Alleles

HGVS	Amino-acid change
ENST00000704074.1:c.294_297delinsGGCC
ENST00000283179.14:c.616_619delinsGGCC	ENSP00000283179.10:p.Gly206=
ENST00000444376.7:c.616_619delinsGGCC	ENSP00000393151.2:p.Gly206=
ENST00000476241.2:n.801_804delinsGGCC
ENST00000638475.1:c.400_403delinsGGCC	ENSP00000491305.1:p.Gly134=
ENST00000638952.1:n.847_850delinsGGCC
ENST00000640218.2:c.616_619delinsGGCC MANE Select	ENSP00000491215.1:p.Gly206=
ENST00000640306.1:c.616_619delinsGGCC	ENSP00000491685.1:p.Gly206=
ENST00000640440.1:c.316_319delinsGGCC	ENSP00000491263.1:p.Gly106=
ENST00000649899.1:n.840_843delinsGGCC
ENST00000283179.13:c.616_619delinsGGCC	ENSP00000283179.9:p.Gly206=
ENST00000444376.6:c.616_619delinsGGCC	ENSP00000393151.2:p.Gly206=
ENST00000476241.1:n.800_803delinsGGCC
NM_004501.3:c.616_619delinsGGCC	NP_004492.2:p.Gly206=
NM_031844.2:c.616_619delinsGGCC	NP_114032.2:p.Gly206=
NM_031844.3:c.616_619delinsGGCC MANE Select	NP_114032.2:p.Gly206=