Canonical Allele Identifier: CA1546376951

Gene: ITGA2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.53055696G= , CM000667.2:g.53055696G=	GRCh38
NC_000005.9:g.52351526G= , CM000667.1:g.52351526G=	GRCh37
NC_000005.8:g.52387283G=	NCBI36
NG_008330.1:g.71371G=
NG_008330.2:g.71371G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296585.10:c.930+8G= MANE Select	ENSP00000296585.5:n.930+8G=
ENST00000296585.9:c.930+8G=	ENSP00000296585.5:n.930+8G=
ENST00000503810.6:c.*274+8G=	ENSP00000426489.1:n.*274+8G=
ENST00000509814.5:c.930+8G=	ENSP00000424397.1:n.930+8G=
ENST00000509960.5:c.930+8G=	ENSP00000424642.1:n.930+8G=
ENST00000510722.1:c.930+8G=	ENSP00000422145.1:n.930+8G=
ENST00000513685.5:c.*644+8G=	ENSP00000422095.1:n.*644+8G=
NM_002203.3:c.930+8G=	NP_002194.2:n.930+8G=
NR_073103.1:n.1073+8G=
NR_073104.1:n.1073+8G=
NR_073105.1:n.1073+8G=
NR_073106.1:n.1073+8G=
NR_073107.1:n.952+8G=
NM_002203.4:c.930+8G= MANE Select	NP_002194.2:n.930+8G=
NR_073103.2:n.1047+8G=
NR_073104.2:n.1047+8G=
NR_073105.2:n.1047+8G=
NR_073106.2:n.1047+8G=
NR_073107.2:n.926+8G=