Canonical Allele Identifier: CA1546376903
Gene: ITGA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.53055568G= , CM000667.2:g.53055568G= GRCh38
NC_000005.9:g.52351398G= , CM000667.1:g.52351398G= GRCh37
NC_000005.8:g.52387155G= NCBI36
NG_008330.1:g.71243G=
NG_008330.2:g.71243G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000296585.10:c.810G= MANE Select ENSP00000296585.5:p.Gly270=
ENST00000296585.9:c.810G= ENSP00000296585.5:p.Gly270=
ENST00000503810.6:c.*154G= ENSP00000426489.1:n.*154G=
ENST00000509814.5:c.810G= ENSP00000424397.1:p.Gly270=
ENST00000509960.5:c.810G= ENSP00000424642.1:p.Gly270=
ENST00000510722.1:c.810G= ENSP00000422145.1:p.Gly270=
ENST00000513685.5:c.*524G= ENSP00000422095.1:n.*524G=
NM_002203.3:c.810G= NP_002194.2:p.Gly270=
NR_073103.1:n.953G=
NR_073104.1:n.953G=
NR_073105.1:n.953G=
NR_073106.1:n.953G=
NR_073107.1:n.832G=
NM_002203.4:c.810G= MANE Select NP_002194.2:p.Gly270=
NR_073103.2:n.927G=
NR_073104.2:n.927G=
NR_073105.2:n.927G=
NR_073106.2:n.927G=
NR_073107.2:n.806G=