Canonical Allele Identifier: CA444163488

Gene: ITGA2

Linked Data

• MyVariant Identifiers: chr5:g.52351494C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.53055664C>T , CM000667.2:g.53055664C>T	GRCh38
NC_000005.9:g.52351494C>T , CM000667.1:g.52351494C>T	GRCh37
NC_000005.8:g.52387251C>T	NCBI36
NG_008330.1:g.71339C>T
NG_008330.2:g.71339C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296585.10:c.906C>T MANE Select	ENSP00000296585.5:p.Asp302=
ENST00000296585.9:c.906C>T	ENSP00000296585.5:p.Asp302=
ENST00000503810.6:c.*250C>T	ENSP00000426489.1:n.*250C>T
ENST00000509814.5:c.906C>T	ENSP00000424397.1:p.Asp302=
ENST00000509960.5:c.906C>T	ENSP00000424642.1:p.Asp302=
ENST00000510722.1:c.906C>T	ENSP00000422145.1:p.Asp302=
ENST00000513685.5:c.*620C>T	ENSP00000422095.1:n.*620C>T
NM_002203.3:c.906C>T	NP_002194.2:p.Asp302=
NR_073103.1:n.1049C>T
NR_073104.1:n.1049C>T
NR_073105.1:n.1049C>T
NR_073106.1:n.1049C>T
NR_073107.1:n.928C>T
NM_002203.4:c.906C>T MANE Select	NP_002194.2:p.Asp302=
NR_073103.2:n.1023C>T
NR_073104.2:n.1023C>T
NR_073105.2:n.1023C>T
NR_073106.2:n.1023C>T
NR_073107.2:n.902C>T