Canonical Allele Identifier: CA1546375129

Gene: ITGA2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.53051539C= , CM000667.2:g.53051539C=	GRCh38
NC_000005.9:g.52347369C= , CM000667.1:g.52347369C=	GRCh37
NC_000005.8:g.52383126C=	NCBI36
NG_008330.1:g.67214C=
NG_008330.2:g.67214C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296585.10:c.759C= MANE Select	ENSP00000296585.5:p.Phe253=
ENST00000296585.9:c.759C=	ENSP00000296585.5:p.Phe253=
ENST00000503810.6:c.*103C=	ENSP00000426489.1:n.*103C=
ENST00000509814.5:c.759C=	ENSP00000424397.1:p.Phe253=
ENST00000509960.5:c.759C=	ENSP00000424642.1:p.Phe253=
ENST00000510722.1:c.759C=	ENSP00000422145.1:p.Phe253=
ENST00000513685.5:c.*473C=	ENSP00000422095.1:n.*473C=
NM_002203.3:c.759C=	NP_002194.2:p.Phe253=
NR_073103.1:n.902C=
NR_073104.1:n.902C=
NR_073105.1:n.902C=
NR_073106.1:n.902C=
NR_073107.1:n.781C=
NM_002203.4:c.759C= MANE Select	NP_002194.2:p.Phe253=
NR_073103.2:n.876C=
NR_073104.2:n.876C=
NR_073105.2:n.876C=
NR_073106.2:n.876C=
NR_073107.2:n.755C=