Canonical Allele Identifier: CA2261365397

Gene: ITGA2B

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44374767_44374773delinsAGGTTGG , CM000679.2:g.44374767_44374773delinsAGGTTGG	GRCh38
NC_000017.10:g.42452135_42452141delinsAGGTTGG , CM000679.1:g.42452135_42452141delinsAGGTTGG	GRCh37
NC_000017.9:g.39807661_39807667delinsAGGTTGG	NCBI36
NG_008331.1:g.19733_19739delinsCCAACCT , LRG_479:g.19733_19739delinsCCAACCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262407.6:c.2842-13_2842-7delinsCCAACCT MANE Select	ENSP00000262407.5:n.2842-13_2842-7delinsCCAACCT
ENST00000648408.1:c.2273-13_2273-7delinsCCAACCT
ENST00000262407.5:c.2842-13_2842-7delinsCCAACCT	ENSP00000262407.5:n.2842-13_2842-7delinsCCAACCT
ENST00000587295.5:c.253+1060_253+1066delinsCCAACCT
ENST00000592462.5:n.2340_2346delinsCCAACCT
NM_000419.3:c.2842-13_2842-7delinsCCAACCT , LRG_479t1:c.2842-13_2842-7delinsCCAACCT	NP_000410.2:n.2842-13_2842-7delinsCCAACCT
XM_011524749.1:c.2841+225_2841+231delinsCCAACCT	XP_011523051.1:n.2841+225_2841+231delinsCCAACCT
XM_011524750.1:c.2842-13_2842-7delinsCCAACCT	XP_011523052.1:n.2842-13_2842-7delinsCCAACCT
NM_000419.4:c.2842-13_2842-7delinsCCAACCT	NP_000410.2:n.2842-13_2842-7delinsCCAACCT
NM_000419.5:c.2842-13_2842-7delinsCCAACCT MANE Select	NP_000410.2:n.2842-13_2842-7delinsCCAACCT