Canonical Allele Identifier: CA2391873769

Gene: ITGB2

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.44889289_44889290delinsAG , CM000683.2:g.44889289_44889290delinsAG	GRCh38
NC_000021.8:g.46309204_46309205delinsAG , CM000683.1:g.46309204_46309205delinsAG	GRCh37
NC_000021.7:g.45133632_45133633delinsAG	NCBI36
NG_007270.2:g.44549_44550delinsCT , LRG_76:g.44549_44550delinsCT

Transcript Alleles

HGVS	Amino-acid change
ENST00000696946.1:n.1070_1071delinsCT
ENST00000302347.10:c.1935_1936delinsCT	ENSP00000303242.6:p.Pro645=
ENST00000652462.1:c.1863_1864delinsCT MANE Select	ENSP00000498780.1:p.Pro621=
ENST00000302347.9:c.1863_1864delinsCT	ENSP00000303242.5:p.Pro621=
ENST00000355153.8:c.1863_1864delinsCT	ENSP00000347279.4:p.Pro621=
ENST00000397850.6:c.1863_1864delinsCT	ENSP00000380948.2:p.Pro621=
ENST00000397852.5:c.1863_1864delinsCT	ENSP00000380950.1:p.Pro621=
ENST00000397854.7:c.1692_1693delinsCT	ENSP00000380952.3:p.Pro564=
ENST00000397857.5:c.1863_1864delinsCT	ENSP00000380955.1:p.Pro621=
ENST00000475170.5:n.1263_1264delinsCT
ENST00000498666.5:n.3919_3920delinsCT
ENST00000523323.5:c.*1690_*1691delinsCT	ENSP00000427732.1:n.*1690_*1691delinsCT
ENST00000610622.4:c.*554_*555delinsCT	ENSP00000480700.1:n.*554_*555delinsCT
NM_000211.4:c.1863_1864delinsCT	NP_000202.3:p.Pro621=
NM_001127491.2:c.1863_1864delinsCT	NP_001120963.2:p.Pro621=
NM_001303238.1:c.1656_1657delinsCT	NP_001290167.1:p.Pro552=
XM_006724001.1:c.1656_1657delinsCT	XP_006724064.1:p.Pro552=
XM_006724001.2:c.1656_1657delinsCT	XP_006724064.1:p.Pro552=
NM_000211.5:c.1863_1864delinsCT MANE Select	NP_000202.3:p.Pro621=
NM_001127491.3:c.1863_1864delinsCT	NP_001120963.2:p.Pro621=
NM_001303238.2:c.1656_1657delinsCT	NP_001290167.1:p.Pro552=