Canonical Allele Identifier: CA2261364262

Gene: ITGA2B

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44372212_44372213delinsAG , CM000679.2:g.44372212_44372213delinsAG	GRCh38
NC_000017.10:g.42449580_42449581delinsAG , CM000679.1:g.42449580_42449581delinsAG	GRCh37
NC_000017.9:g.39805106_39805107delinsAG	NCBI36
NG_008331.1:g.22293_22294delinsCT , LRG_479:g.22293_22294delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262407.6:c.*151_*152delinsCT MANE Select	ENSP00000262407.5:n.*151_*152delinsCT
ENST00000648408.1:c.2585_2586delinsCT
ENST00000262407.5:c.*151_*152delinsCT	ENSP00000262407.5:n.*151_*152delinsCT
ENST00000587295.5:c.464_465delinsCT
ENST00000588098.1:c.248_249delinsCT
NM_000419.3:c.*151_*152delinsCT , LRG_479t1:c.*151_*152delinsCT	NP_000410.2:n.*151_*152delinsCT
XM_011524749.1:c.*151_*152delinsCT	XP_011523051.1:n.*151_*152delinsCT
XM_011524750.1:c.*151_*152delinsCT	XP_011523052.1:n.*151_*152delinsCT
NM_000419.4:c.*151_*152delinsCT	NP_000410.2:n.*151_*152delinsCT
NM_000419.5:c.*151_*152delinsCT MANE Select	NP_000410.2:n.*151_*152delinsCT