Canonical Allele Identifier: CA1900540418

Gene: ITGB1

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.32920338G= , CM000672.2:g.32920338G=	GRCh38
NC_000010.10:g.33209266G= , CM000672.1:g.33209266G=	GRCh37
NC_000010.9:g.33249272G=	NCBI36
NG_029012.1:g.43028C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000423113.6:c.1176C=	ENSP00000388694.1:p.Gly392=
ENST00000302278.8:c.1176C= MANE Select	ENSP00000303351.3:p.Gly392=
ENST00000417122.7:c.1176C=	ENSP00000404546.3:p.Gly392=
ENST00000437302.6:c.1176C=	ENSP00000398029.2:p.Gly392=
ENST00000474568.6:c.1200C=	ENSP00000420282.2:p.Gly400=
ENST00000488427.2:c.1005C=	ENSP00000417508.2:p.Gly335=
ENST00000488494.6:c.1185C=	ENSP00000418725.2:p.Gly395=
ENST00000609742.3:c.1176C=	ENSP00000503306.1:p.Gly392=
ENST00000676460.1:c.1176C=	ENSP00000504641.1:p.Gly392=
ENST00000676623.1:n.3156C=
ENST00000676659.1:c.1176C=	ENSP00000502979.1:p.Gly392=
ENST00000676895.1:c.*165C=	ENSP00000504454.1:n.*165C=
ENST00000676964.1:c.1005C=	ENSP00000504267.1:p.Gly335=
ENST00000677310.1:c.1176C=	ENSP00000504508.1:p.Gly392=
ENST00000677363.1:c.1200C=	ENSP00000504791.1:p.Gly400=
ENST00000677999.1:c.1176C=	ENSP00000503546.1:p.Gly392=
ENST00000678120.1:c.*48C=	ENSP00000504784.1:n.*48C=
ENST00000678479.1:c.*982C=	ENSP00000503110.1:n.*982C=
ENST00000678591.1:c.1164C=	ENSP00000502883.1:p.Gly388=
ENST00000678701.1:c.1176C=	ENSP00000504205.1:p.Gly392=
ENST00000678766.1:c.1176C=	ENSP00000503538.1:p.Gly392=
ENST00000678943.1:c.1176C=	ENSP00000503916.1:p.Gly392=
ENST00000678952.1:c.1176C=	ENSP00000504444.1:p.Gly392=
ENST00000678989.1:c.1176C=	ENSP00000502882.1:p.Gly392=
ENST00000679187.1:c.1005C=	ENSP00000504012.1:p.Gly335=
ENST00000302278.7:c.1176C=	ENSP00000303351.3:p.Gly392=
ENST00000396033.6:c.1176C=	ENSP00000379350.2:p.Gly392=
ENST00000423113.5:c.1176C=	ENSP00000388694.1:p.Gly392=
NM_002211.3:c.1176C=	NP_002202.2:p.Gly392=
NM_033668.2:c.1176C=	NP_391988.1:p.Gly392=
NM_133376.2:c.1176C=	NP_596867.1:p.Gly392=
XM_005252448.1:c.1176C=	XP_005252505.1:p.Gly392=
NM_002211.4:c.1176C= MANE Select	NP_002202.2:p.Gly392=
NM_133376.3:c.1176C=	NP_596867.1:p.Gly392=