Canonical Allele Identifier: CA1546376943

Gene: ITGA2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.53055676G= , CM000667.2:g.53055676G=	GRCh38
NC_000005.9:g.52351506G= , CM000667.1:g.52351506G=	GRCh37
NC_000005.8:g.52387263G=	NCBI36
NG_008330.1:g.71351G=
NG_008330.2:g.71351G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296585.10:c.918G= MANE Select	ENSP00000296585.5:p.Arg306=
ENST00000296585.9:c.918G=	ENSP00000296585.5:p.Arg306=
ENST00000503810.6:c.*262G=	ENSP00000426489.1:n.*262G=
ENST00000509814.5:c.918G=	ENSP00000424397.1:p.Arg306=
ENST00000509960.5:c.918G=	ENSP00000424642.1:p.Arg306=
ENST00000510722.1:c.918G=	ENSP00000422145.1:p.Arg306=
ENST00000513685.5:c.*632G=	ENSP00000422095.1:n.*632G=
NM_002203.3:c.918G=	NP_002194.2:p.Arg306=
NR_073103.1:n.1061G=
NR_073104.1:n.1061G=
NR_073105.1:n.1061G=
NR_073106.1:n.1061G=
NR_073107.1:n.940G=
NM_002203.4:c.918G= MANE Select	NP_002194.2:p.Arg306=
NR_073103.2:n.1035G=
NR_073104.2:n.1035G=
NR_073105.2:n.1035G=
NR_073106.2:n.1035G=
NR_073107.2:n.914G=