Canonical Allele Identifier: CA1546376874

Gene: ITGA2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.53055496A= , CM000667.2:g.53055496A=	GRCh38
NC_000005.9:g.52351326A= , CM000667.1:g.52351326A=	GRCh37
NC_000005.8:g.52387083A=	NCBI36
NG_008330.1:g.71171A=
NG_008330.2:g.71171A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000296585.10:c.780-42A= MANE Select	ENSP00000296585.5:n.780-42A=
ENST00000296585.9:c.780-42A=	ENSP00000296585.5:n.780-42A=
ENST00000503810.6:c.*124-42A=	ENSP00000426489.1:n.*124-42A=
ENST00000509814.5:c.780-42A=	ENSP00000424397.1:n.780-42A=
ENST00000509960.5:c.780-42A=	ENSP00000424642.1:n.780-42A=
ENST00000510722.1:c.780-42A=	ENSP00000422145.1:n.780-42A=
ENST00000513685.5:c.*494-42A=	ENSP00000422095.1:n.*494-42A=
NM_002203.3:c.780-42A=	NP_002194.2:n.780-42A=
NR_073103.1:n.923-42A=
NR_073104.1:n.923-42A=
NR_073105.1:n.923-42A=
NR_073106.1:n.923-42A=
NR_073107.1:n.802-42A=
NM_002203.4:c.780-42A= MANE Select	NP_002194.2:n.780-42A=
NR_073103.2:n.897-42A=
NR_073104.2:n.897-42A=
NR_073105.2:n.897-42A=
NR_073106.2:n.897-42A=
NR_073107.2:n.776-42A=