Canonical Allele Identifier: CA1399033558

Gene: ITGB5

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.124886032A= , CM000665.2:g.124886032A=	GRCh38
NC_000003.11:g.124604879A= , CM000665.1:g.124604879A=	GRCh37
NC_000003.10:g.126087569A=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000296181.9:c.70+899T= MANE Select	ENSP00000296181.4:n.70+899T=
ENST00000296181.8:c.70+899T=	ENSP00000296181.4:n.70+899T=
ENST00000465464.5:c.-255+1568T=	ENSP00000418079.2:n.-255+1568T=
ENST00000483168.5:c.-255+1568T=	ENSP00000419198.2:n.-255+1568T=
ENST00000608657.5:c.-254-12501T=	ENSP00000477230.1:n.-254-12501T=
NM_002213.4:c.70+899T=	NP_002204.2:n.70+899T=
XM_005247436.2:c.70+899T=	XP_005247493.1:n.70+899T=
XM_006713630.2:c.70+899T=	XP_006713693.1:n.70+899T=
NM_001354764.1:c.-254-12501T=	NP_001341693.1:n.-254-12501T=
NM_001354765.1:c.-255+1568T=	NP_001341694.1:n.-255+1568T=
NM_001354766.1:c.-254-12501T=	NP_001341695.1:n.-254-12501T=
XM_005247436.3:c.70+899T=	XP_005247493.1:n.70+899T=
XM_006713630.3:c.70+899T=	XP_006713693.1:n.70+899T=
XM_017006354.2:c.70+899T=	XP_016861843.1:n.70+899T=
XM_017006355.1:c.-255+1568T=	XP_016861844.1:n.-255+1568T=
NM_002213.5:c.70+899T= MANE Select	NP_002204.2:n.70+899T=
NM_001354764.2:c.-254-12501T=	NP_001341693.1:n.-254-12501T=
NM_001354766.2:c.-254-12501T=	NP_001341695.1:n.-254-12501T=