Canonical Allele Identifier: CA1399033557
Gene: ITGB5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.124886031C= , CM000665.2:g.124886031C= GRCh38
NC_000003.11:g.124604878C= , CM000665.1:g.124604878C= GRCh37
NC_000003.10:g.126087568C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000296181.9:c.70+900G= MANE Select ENSP00000296181.4:n.70+900G=
ENST00000296181.8:c.70+900G= ENSP00000296181.4:n.70+900G=
ENST00000465464.5:c.-255+1569G= ENSP00000418079.2:n.-255+1569G=
ENST00000483168.5:c.-255+1569G= ENSP00000419198.2:n.-255+1569G=
ENST00000608657.5:c.-254-12500G= ENSP00000477230.1:n.-254-12500G=
NM_002213.4:c.70+900G= NP_002204.2:n.70+900G=
XM_005247436.2:c.70+900G= XP_005247493.1:n.70+900G=
XM_006713630.2:c.70+900G= XP_006713693.1:n.70+900G=
NM_001354764.1:c.-254-12500G= NP_001341693.1:n.-254-12500G=
NM_001354765.1:c.-255+1569G= NP_001341694.1:n.-255+1569G=
NM_001354766.1:c.-254-12500G= NP_001341695.1:n.-254-12500G=
XM_005247436.3:c.70+900G= XP_005247493.1:n.70+900G=
XM_006713630.3:c.70+900G= XP_006713693.1:n.70+900G=
XM_017006354.2:c.70+900G= XP_016861843.1:n.70+900G=
XM_017006355.1:c.-255+1569G= XP_016861844.1:n.-255+1569G=
NM_002213.5:c.70+900G= MANE Select NP_002204.2:n.70+900G=
NM_001354764.2:c.-254-12500G= NP_001341693.1:n.-254-12500G=
NM_001354766.2:c.-254-12500G= NP_001341695.1:n.-254-12500G=