Canonical Allele Identifier: CA1546376913

Gene: ITGA2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.53055593G= , CM000667.2:g.53055593G=	GRCh38
NC_000005.9:g.52351423G= , CM000667.1:g.52351423G=	GRCh37
NC_000005.8:g.52387180G=	NCBI36
NG_008330.1:g.71268G=
NG_008330.2:g.71268G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296585.10:c.835G= MANE Select	ENSP00000296585.5:p.Val279=
ENST00000296585.9:c.835G=	ENSP00000296585.5:p.Val279=
ENST00000503810.6:c.*179G=	ENSP00000426489.1:n.*179G=
ENST00000509814.5:c.835G=	ENSP00000424397.1:p.Val279=
ENST00000509960.5:c.835G=	ENSP00000424642.1:p.Val279=
ENST00000510722.1:c.835G=	ENSP00000422145.1:p.Val279=
ENST00000513685.5:c.*549G=	ENSP00000422095.1:n.*549G=
NM_002203.3:c.835G=	NP_002194.2:p.Val279=
NR_073103.1:n.978G=
NR_073104.1:n.978G=
NR_073105.1:n.978G=
NR_073106.1:n.978G=
NR_073107.1:n.857G=
NM_002203.4:c.835G= MANE Select	NP_002194.2:p.Val279=
NR_073103.2:n.952G=
NR_073104.2:n.952G=
NR_073105.2:n.952G=
NR_073106.2:n.952G=
NR_073107.2:n.831G=