Canonical Allele Identifier: CA1546376941

Gene: ITGA2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.53055671C= , CM000667.2:g.53055671C=	GRCh38
NC_000005.9:g.52351501C= , CM000667.1:g.52351501C=	GRCh37
NC_000005.8:g.52387258C=	NCBI36
NG_008330.1:g.71346C=
NG_008330.2:g.71346C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296585.10:c.913C= MANE Select	ENSP00000296585.5:p.Leu305=
ENST00000296585.9:c.913C=	ENSP00000296585.5:p.Leu305=
ENST00000503810.6:c.*257C=	ENSP00000426489.1:n.*257C=
ENST00000509814.5:c.913C=	ENSP00000424397.1:p.Leu305=
ENST00000509960.5:c.913C=	ENSP00000424642.1:p.Leu305=
ENST00000510722.1:c.913C=	ENSP00000422145.1:p.Leu305=
ENST00000513685.5:c.*627C=	ENSP00000422095.1:n.*627C=
NM_002203.3:c.913C=	NP_002194.2:p.Leu305=
NR_073103.1:n.1056C=
NR_073104.1:n.1056C=
NR_073105.1:n.1056C=
NR_073106.1:n.1056C=
NR_073107.1:n.935C=
NM_002203.4:c.913C= MANE Select	NP_002194.2:p.Leu305=
NR_073103.2:n.1030C=
NR_073104.2:n.1030C=
NR_073105.2:n.1030C=
NR_073106.2:n.1030C=
NR_073107.2:n.909C=