Canonical Allele Identifier: CA645584248

Gene: ITGA2B

Linked Data

• COSMIC: COSM1302886

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44377702_44377703delinsTA , CM000679.2:g.44377702_44377703delinsTA	GRCh38
NC_000017.10:g.42455070_42455071delinsTA , CM000679.1:g.42455070_42455071delinsTA	GRCh37
NC_000017.9:g.39810596_39810597delinsTA	NCBI36
NG_008331.1:g.16803_16804delinsTA , LRG_479:g.16803_16804delinsTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262407.6:c.2182_2183delinsTA MANE Select	ENSP00000262407.5:p.Ala728Tyr
ENST00000648408.1:c.1613_1614delinsTA
ENST00000262407.5:c.2182_2183delinsTA	ENSP00000262407.5:p.Ala728Tyr
ENST00000592462.5:n.977_978delinsTA
NM_000419.3:c.2182_2183delinsTA , LRG_479t1:c.2182_2183delinsTA	NP_000410.2:p.Ala728Tyr
XM_011524749.1:c.2182_2183delinsTA	XP_011523051.1:p.Ala728Tyr
XM_011524750.1:c.2182_2183delinsTA	XP_011523052.1:p.Ala728Tyr
NM_000419.4:c.2182_2183delinsTA	NP_000410.2:p.Ala728Tyr
NM_000419.5:c.2182_2183delinsTA MANE Select	NP_000410.2:p.Ala728Tyr