Canonical Allele Identifier: CA2391875714

Gene: ITGB2

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.44893097_44893108delinsAGCACCCTCTCG , CM000683.2:g.44893097_44893108delinsAGCACCCTCTCG	GRCh38
NC_000021.8:g.46313012_46313023delinsAGCACCCTCTCG , CM000683.1:g.46313012_46313023delinsAGCACCCTCTCG	GRCh37
NC_000021.7:g.45137440_45137451delinsAGCACCCTCTCG	NCBI36
NG_007270.2:g.40731_40742delinsCGAGAGGGTGCT , LRG_76:g.40731_40742delinsCGAGAGGGTGCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302347.10:c.1296+296_1296+307delinsCGAGAGGGTGCT	ENSP00000303242.6:n.1296+296_1296+307delinsCGAGAGGGTGCT
ENST00000652462.1:c.1224+296_1224+307delinsCGAGAGGGTGCT MANE Select	ENSP00000498780.1:n.1224+296_1224+307delinsCGAGAGGGTGCT
ENST00000302347.9:c.1224+296_1224+307delinsCGAGAGGGTGCT	ENSP00000303242.5:n.1224+296_1224+307delinsCGAGAGGGTGCT
ENST00000355153.8:c.1224+296_1224+307delinsCGAGAGGGTGCT	ENSP00000347279.4:n.1224+296_1224+307delinsCGAGAGGGTGCT
ENST00000397850.6:c.1224+296_1224+307delinsCGAGAGGGTGCT	ENSP00000380948.2:n.1224+296_1224+307delinsCGAGAGGGTGCT
ENST00000397852.5:c.1224+296_1224+307delinsCGAGAGGGTGCT	ENSP00000380950.1:n.1224+296_1224+307delinsCGAGAGGGTGCT
ENST00000397854.7:c.1053+296_1053+307delinsCGAGAGGGTGCT	ENSP00000380952.3:n.1053+296_1053+307delinsCGAGAGGGTGCT
ENST00000397857.5:c.1224+296_1224+307delinsCGAGAGGGTGCT	ENSP00000380955.1:n.1224+296_1224+307delinsCGAGAGGGTGCT
ENST00000475170.5:n.624+296_624+307delinsCGAGAGGGTGCT
ENST00000498666.5:n.3089_3100delinsCGAGAGGGTGCT
ENST00000523323.5:c.*1051+296_*1051+307delinsCGAGAGGGTGCT	ENSP00000427732.1:n.*1051+296_*1051+307delinsCGAGAGGGTGCT
ENST00000610622.4:c.1053+296_1053+307delinsCGAGAGGGTGCT	ENSP00000480700.1:n.1053+296_1053+307delinsCGAGAGGGTGCT
NM_000211.4:c.1224+296_1224+307delinsCGAGAGGGTGCT	NP_000202.3:n.1224+296_1224+307delinsCGAGAGGGTGCT
NM_001127491.2:c.1224+296_1224+307delinsCGAGAGGGTGCT	NP_001120963.2:n.1224+296_1224+307delinsCGAGAGGGTGCT
NM_001303238.1:c.1017+296_1017+307delinsCGAGAGGGTGCT	NP_001290167.1:n.1017+296_1017+307delinsCGAGAGGGTGCT
XM_006724001.1:c.1017+296_1017+307delinsCGAGAGGGTGCT	XP_006724064.1:n.1017+296_1017+307delinsCGAGAGGGTGCT
XM_006724001.2:c.1017+296_1017+307delinsCGAGAGGGTGCT	XP_006724064.1:n.1017+296_1017+307delinsCGAGAGGGTGCT
NM_000211.5:c.1224+296_1224+307delinsCGAGAGGGTGCT MANE Select	NP_000202.3:n.1224+296_1224+307delinsCGAGAGGGTGCT
NM_001127491.3:c.1224+296_1224+307delinsCGAGAGGGTGCT	NP_001120963.2:n.1224+296_1224+307delinsCGAGAGGGTGCT
NM_001303238.2:c.1017+296_1017+307delinsCGAGAGGGTGCT	NP_001290167.1:n.1017+296_1017+307delinsCGAGAGGGTGCT