Canonical Allele Identifier: CA2840396052

Gene: ITGA2B

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44374960_44374961del , CM000679.2:g.44374960_44374961del	GRCh38
NC_000017.10:g.42452328_42452329del , CM000679.1:g.42452328_42452329del	GRCh37
NC_000017.9:g.39807854_39807855del	NCBI36
NG_008331.1:g.19545_19546del , LRG_479:g.19545_19546del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262407.6:c.2841+37_2841+38del MANE Select	ENSP00000262407.5:n.2841+37_2841+38del
ENST00000648408.1:c.2272+37_2272+38del
ENST00000262407.5:c.2841+37_2841+38del	ENSP00000262407.5:n.2841+37_2841+38del
ENST00000587295.5:c.253+872_253+873del
ENST00000592462.5:n.2152_2153del
NM_000419.3:c.2841+37_2841+38del , LRG_479t1:c.2841+37_2841+38del	NP_000410.2:n.2841+37_2841+38del
XM_011524749.1:c.2841+37_2841+38del	XP_011523051.1:n.2841+37_2841+38del
XM_011524750.1:c.2841+37_2841+38del	XP_011523052.1:n.2841+37_2841+38del
NM_000419.4:c.2841+37_2841+38del	NP_000410.2:n.2841+37_2841+38del
NM_000419.5:c.2841+37_2841+38del MANE Select	NP_000410.2:n.2841+37_2841+38del