Canonical Allele Identifier: CA359684613
Gene: ITGA2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.53055635A>C , CM000667.2:g.53055635A>C GRCh38
NC_000005.9:g.52351465A>C , CM000667.1:g.52351465A>C GRCh37
NC_000005.8:g.52387222A>C NCBI36
NG_008330.1:g.71310A>C
NG_008330.2:g.71310A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000296585.10:c.877A>C MANE Select ENSP00000296585.5:p.Lys293Gln
ENST00000296585.9:c.877A>C ENSP00000296585.5:p.Lys293Gln
ENST00000503810.6:c.*221A>C ENSP00000426489.1:n.*221A>C
ENST00000509814.5:c.877A>C ENSP00000424397.1:p.Lys293Gln
ENST00000509960.5:c.877A>C ENSP00000424642.1:p.Lys293Gln
ENST00000510722.1:c.877A>C ENSP00000422145.1:p.Lys293Gln
ENST00000513685.5:c.*591A>C ENSP00000422095.1:n.*591A>C
NM_002203.3:c.877A>C NP_002194.2:p.Lys293Gln
NR_073103.1:n.1020A>C
NR_073104.1:n.1020A>C
NR_073105.1:n.1020A>C
NR_073106.1:n.1020A>C
NR_073107.1:n.899A>C
NM_002203.4:c.877A>C MANE Select NP_002194.2:p.Lys293Gln
NR_073103.2:n.994A>C
NR_073104.2:n.994A>C
NR_073105.2:n.994A>C
NR_073106.2:n.994A>C
NR_073107.2:n.873A>C