Canonical Allele Identifier: CA444163361

Gene: ITGA2

Linked Data

• MyVariant Identifiers: chr5:g.52351416A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.53055586A>G , CM000667.2:g.53055586A>G	GRCh38
NC_000005.9:g.52351416A>G , CM000667.1:g.52351416A>G	GRCh37
NC_000005.8:g.52387173A>G	NCBI36
NG_008330.1:g.71261A>G
NG_008330.2:g.71261A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296585.10:c.828A>G MANE Select	ENSP00000296585.5:p.Lys276=
ENST00000296585.9:c.828A>G	ENSP00000296585.5:p.Lys276=
ENST00000503810.6:c.*172A>G	ENSP00000426489.1:n.*172A>G
ENST00000509814.5:c.828A>G	ENSP00000424397.1:p.Lys276=
ENST00000509960.5:c.828A>G	ENSP00000424642.1:p.Lys276=
ENST00000510722.1:c.828A>G	ENSP00000422145.1:p.Lys276=
ENST00000513685.5:c.*542A>G	ENSP00000422095.1:n.*542A>G
NM_002203.3:c.828A>G	NP_002194.2:p.Lys276=
NR_073103.1:n.971A>G
NR_073104.1:n.971A>G
NR_073105.1:n.971A>G
NR_073106.1:n.971A>G
NR_073107.1:n.850A>G
NM_002203.4:c.828A>G MANE Select	NP_002194.2:p.Lys276=
NR_073103.2:n.945A>G
NR_073104.2:n.945A>G
NR_073105.2:n.945A>G
NR_073106.2:n.945A>G
NR_073107.2:n.824A>G