Canonical Allele Identifier: CA2261365325

Gene: ITGA2B

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44374621_44374622delinsCT , CM000679.2:g.44374621_44374622delinsCT	GRCh38
NC_000017.10:g.42451989_42451990delinsCT , CM000679.1:g.42451989_42451990delinsCT	GRCh37
NC_000017.9:g.39807515_39807516delinsCT	NCBI36
NG_008331.1:g.19884_19885delinsAG , LRG_479:g.19884_19885delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262407.6:c.2943+37_2943+38delinsAG MANE Select	ENSP00000262407.5:n.2943+37_2943+38delinsAG
ENST00000648408.1:c.2374+37_2374+38delinsAG
ENST00000262407.5:c.2943+37_2943+38delinsAG	ENSP00000262407.5:n.2943+37_2943+38delinsAG
ENST00000587295.5:c.253+1211_253+1212delinsAG
ENST00000588098.1:c.37+37_37+38delinsAG
ENST00000592462.5:n.2491_2492delinsAG
NM_000419.3:c.2943+37_2943+38delinsAG , LRG_479t1:c.2943+37_2943+38delinsAG	NP_000410.2:n.2943+37_2943+38delinsAG
XM_011524749.1:c.2842-152_2842-151delinsAG	XP_011523051.1:n.2842-152_2842-151delinsAG
XM_011524750.1:c.2943+37_2943+38delinsAG	XP_011523052.1:n.2943+37_2943+38delinsAG
NM_000419.4:c.2943+37_2943+38delinsAG	NP_000410.2:n.2943+37_2943+38delinsAG
NM_000419.5:c.2943+37_2943+38delinsAG MANE Select	NP_000410.2:n.2943+37_2943+38delinsAG