Canonical Allele Identifier: CA2809589787

Gene: ITGA2B

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44374948_44374949insCCTG , CM000679.2:g.44374948_44374949insCCTG	GRCh38
NC_000017.10:g.42452316_42452317insCCTG , CM000679.1:g.42452316_42452317insCCTG	GRCh37
NC_000017.9:g.39807842_39807843insCCTG	NCBI36
NG_008331.1:g.19558_19559insAGGC , LRG_479:g.19558_19559insAGGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262407.6:c.2841+50_2841+51insAGGC MANE Select	ENSP00000262407.5:n.2841+50_2841+51insAGGC
ENST00000648408.1:c.2272+50_2272+51insAGGC
ENST00000262407.5:c.2841+50_2841+51insAGGC	ENSP00000262407.5:n.2841+50_2841+51insAGGC
ENST00000587295.5:c.253+885_253+886insAGGC
ENST00000592462.5:n.2165_2166insAGGC
NM_000419.3:c.2841+50_2841+51insAGGC , LRG_479t1:c.2841+50_2841+51insAGGC	NP_000410.2:n.2841+50_2841+51insAGGC
XM_011524749.1:c.2841+50_2841+51insAGGC	XP_011523051.1:n.2841+50_2841+51insAGGC
XM_011524750.1:c.2841+50_2841+51insAGGC	XP_011523052.1:n.2841+50_2841+51insAGGC
NM_000419.4:c.2841+50_2841+51insAGGC	NP_000410.2:n.2841+50_2841+51insAGGC
NM_000419.5:c.2841+50_2841+51insAGGC MANE Select	NP_000410.2:n.2841+50_2841+51insAGGC