Canonical Allele Identifier: CA2809589789

Gene: ITGA2B

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44374952_44374953insGCC , CM000679.2:g.44374952_44374953insGCC	GRCh38
NC_000017.10:g.42452320_42452321insGCC , CM000679.1:g.42452320_42452321insGCC	GRCh37
NC_000017.9:g.39807846_39807847insGCC	NCBI36
NG_008331.1:g.19553_19554insGGC , LRG_479:g.19553_19554insGGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262407.6:c.2841+45_2841+46insGGC MANE Select	ENSP00000262407.5:n.2841+45_2841+46insGGC
ENST00000648408.1:c.2272+45_2272+46insGGC
ENST00000262407.5:c.2841+45_2841+46insGGC	ENSP00000262407.5:n.2841+45_2841+46insGGC
ENST00000587295.5:c.253+880_253+881insGGC
ENST00000592462.5:n.2160_2161insGGC
NM_000419.3:c.2841+45_2841+46insGGC , LRG_479t1:c.2841+45_2841+46insGGC	NP_000410.2:n.2841+45_2841+46insGGC
XM_011524749.1:c.2841+45_2841+46insGGC	XP_011523051.1:n.2841+45_2841+46insGGC
XM_011524750.1:c.2841+45_2841+46insGGC	XP_011523052.1:n.2841+45_2841+46insGGC
NM_000419.4:c.2841+45_2841+46insGGC	NP_000410.2:n.2841+45_2841+46insGGC
NM_000419.5:c.2841+45_2841+46insGGC MANE Select	NP_000410.2:n.2841+45_2841+46insGGC