Canonical Allele Identifier: CA2261364352

Gene: ITGA2B

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44372376_44372379delinsTTCA , CM000679.2:g.44372376_44372379delinsTTCA	GRCh38
NC_000017.10:g.42449744_42449747delinsTTCA , CM000679.1:g.42449744_42449747delinsTTCA	GRCh37
NC_000017.9:g.39805270_39805273delinsTTCA	NCBI36
NG_008331.1:g.22127_22130delinsTGAA , LRG_479:g.22127_22130delinsTGAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262407.6:c.3105_3108delinsTGAA MANE Select	ENSP00000262407.5:p.Asp1035=
ENST00000648408.1:c.2419_2422delinsTGAA
ENST00000262407.5:c.3105_3108delinsTGAA	ENSP00000262407.5:p.Asp1035=
ENST00000587295.5:c.298_301delinsTGAA
ENST00000588098.1:c.82_85delinsTGAA
NM_000419.3:c.3105_3108delinsTGAA , LRG_479t1:c.3105_3108delinsTGAA	NP_000410.2:p.Asp1035=
XM_011524749.1:c.3003_3006delinsTGAA	XP_011523051.1:p.Asp1001=
XM_011524750.1:c.2988_2991delinsTGAA	XP_011523052.1:p.Asp996=
NM_000419.4:c.3105_3108delinsTGAA	NP_000410.2:p.Asp1035=
NM_000419.5:c.3105_3108delinsTGAA MANE Select	NP_000410.2:p.Asp1035=