Canonical Allele Identifier: CA2261364355

Gene: ITGA2B

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44372382_44372385delinsATCT , CM000679.2:g.44372382_44372385delinsATCT	GRCh38
NC_000017.10:g.42449750_42449753delinsATCT , CM000679.1:g.42449750_42449753delinsATCT	GRCh37
NC_000017.9:g.39805276_39805279delinsATCT	NCBI36
NG_008331.1:g.22121_22124delinsAGAT , LRG_479:g.22121_22124delinsAGAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262407.6:c.3099_3102delinsAGAT MANE Select	ENSP00000262407.5:p.Glu1033=
ENST00000648408.1:c.2413_2416delinsAGAT
ENST00000262407.5:c.3099_3102delinsAGAT	ENSP00000262407.5:p.Glu1033=
ENST00000587295.5:c.292_295delinsAGAT
ENST00000588098.1:c.76_79delinsAGAT
NM_000419.3:c.3099_3102delinsAGAT , LRG_479t1:c.3099_3102delinsAGAT	NP_000410.2:p.Glu1033=
XM_011524749.1:c.2997_3000delinsAGAT	XP_011523051.1:p.Glu999=
XM_011524750.1:c.2982_2985delinsAGAT	XP_011523052.1:p.Glu994=
NM_000419.4:c.3099_3102delinsAGAT	NP_000410.2:p.Glu1033=
NM_000419.5:c.3099_3102delinsAGAT MANE Select	NP_000410.2:p.Glu1033=