Canonical Allele Identifier: CA2261365305

Gene: ITGA2B

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44374588_44374599delinsTCTGGCTGGGCA , CM000679.2:g.44374588_44374599delinsTCTGGCTGGGCA	GRCh38
NC_000017.10:g.42451956_42451967delinsTCTGGCTGGGCA , CM000679.1:g.42451956_42451967delinsTCTGGCTGGGCA	GRCh37
NC_000017.9:g.39807482_39807493delinsTCTGGCTGGGCA	NCBI36
NG_008331.1:g.19907_19918delinsTGCCCAGCCAGA , LRG_479:g.19907_19918delinsTGCCCAGCCAGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262407.6:c.2943+60_2943+71delinsTGCCCAGCCAGA MANE Select	ENSP00000262407.5:n.2943+60_2943+71delinsTGCCCAGCCAGA
ENST00000648408.1:c.2374+60_2374+71delinsTGCCCAGCCAGA
ENST00000262407.5:c.2943+60_2943+71delinsTGCCCAGCCAGA	ENSP00000262407.5:n.2943+60_2943+71delinsTGCCCAGCCAGA
ENST00000587295.5:c.253+1234_253+1245delinsTGCCCAGCCAGA
ENST00000588098.1:c.37+60_37+71delinsTGCCCAGCCAGA
ENST00000592462.5:n.2514_2525delinsTGCCCAGCCAGA
NM_000419.3:c.2943+60_2943+71delinsTGCCCAGCCAGA , LRG_479t1:c.2943+60_2943+71delinsTGCCCAGCCAGA	NP_000410.2:n.2943+60_2943+71delinsTGCCCAGCCAGA
XM_011524749.1:c.2842-129_2842-118delinsTGCCCAGCCAGA	XP_011523051.1:n.2842-129_2842-118delinsTGCCCAGCCAGA
XM_011524750.1:c.2943+60_2943+71delinsTGCCCAGCCAGA	XP_011523052.1:n.2943+60_2943+71delinsTGCCCAGCCAGA
NM_000419.4:c.2943+60_2943+71delinsTGCCCAGCCAGA	NP_000410.2:n.2943+60_2943+71delinsTGCCCAGCCAGA
NM_000419.5:c.2943+60_2943+71delinsTGCCCAGCCAGA MANE Select	NP_000410.2:n.2943+60_2943+71delinsTGCCCAGCCAGA