Canonical Allele Identifier: CA359684064

Gene: ITGA2

Linked Data

• MyVariant Identifiers: chr5:g.52351390T>A (hg19) ; chr5:g.53055560T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.53055560T>A , CM000667.2:g.53055560T>A	GRCh38
NC_000005.9:g.52351390T>A , CM000667.1:g.52351390T>A	GRCh37
NC_000005.8:g.52387147T>A	NCBI36
NG_008330.1:g.71235T>A
NG_008330.2:g.71235T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296585.10:c.802T>A MANE Select	ENSP00000296585.5:p.Ser268Thr
ENST00000296585.9:c.802T>A	ENSP00000296585.5:p.Ser268Thr
ENST00000503810.6:c.*146T>A	ENSP00000426489.1:n.*146T>A
ENST00000509814.5:c.802T>A	ENSP00000424397.1:p.Ser268Thr
ENST00000509960.5:c.802T>A	ENSP00000424642.1:p.Ser268Thr
ENST00000510722.1:c.802T>A	ENSP00000422145.1:p.Ser268Thr
ENST00000513685.5:c.*516T>A	ENSP00000422095.1:n.*516T>A
NM_002203.3:c.802T>A	NP_002194.2:p.Ser268Thr
NR_073103.1:n.945T>A
NR_073104.1:n.945T>A
NR_073105.1:n.945T>A
NR_073106.1:n.945T>A
NR_073107.1:n.824T>A
NM_002203.4:c.802T>A MANE Select	NP_002194.2:p.Ser268Thr
NR_073103.2:n.919T>A
NR_073104.2:n.919T>A
NR_073105.2:n.919T>A
NR_073106.2:n.919T>A
NR_073107.2:n.798T>A