Canonical Allele Identifier: CA2673816355
Gene: ITGA2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.53055488_53055506del , CM000667.2:g.53055488_53055506del GRCh38
NC_000005.9:g.52351318_52351336del , CM000667.1:g.52351318_52351336del GRCh37
NC_000005.8:g.52387075_52387093del NCBI36
NG_008330.1:g.71163_71181del
NG_008330.2:g.71163_71181del

Transcript Alleles

HGVS Amino-acid Change
ENST00000296585.10:c.780-50_780-32del MANE Select ENSP00000296585.5:n.780-50_780-32del
ENST00000296585.9:c.780-50_780-32del ENSP00000296585.5:n.780-50_780-32del
ENST00000503810.6:c.*124-50_*124-32del ENSP00000426489.1:n.*124-50_*124-32del
ENST00000509814.5:c.780-50_780-32del ENSP00000424397.1:n.780-50_780-32del
ENST00000509960.5:c.780-50_780-32del ENSP00000424642.1:n.780-50_780-32del
ENST00000510722.1:c.780-50_780-32del ENSP00000422145.1:n.780-50_780-32del
ENST00000513685.5:c.*494-50_*494-32del ENSP00000422095.1:n.*494-50_*494-32del
NM_002203.3:c.780-50_780-32del NP_002194.2:n.780-50_780-32del
NR_073103.1:n.923-50_923-32del
NR_073104.1:n.923-50_923-32del
NR_073105.1:n.923-50_923-32del
NR_073106.1:n.923-50_923-32del
NR_073107.1:n.802-50_802-32del
NM_002203.4:c.780-50_780-32del MANE Select NP_002194.2:n.780-50_780-32del
NR_073103.2:n.897-50_897-32del
NR_073104.2:n.897-50_897-32del
NR_073105.2:n.897-50_897-32del
NR_073106.2:n.897-50_897-32del
NR_073107.2:n.776-50_776-32del