Canonical Allele Identifier: CA359684815

Gene: ITGA2

Linked Data

• MyVariant Identifiers: chr5:g.52351496A>G (hg19) ; chr5:g.53055666A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.53055666A>G , CM000667.2:g.53055666A>G	GRCh38
NC_000005.9:g.52351496A>G , CM000667.1:g.52351496A>G	GRCh37
NC_000005.8:g.52387253A>G	NCBI36
NG_008330.1:g.71341A>G
NG_008330.2:g.71341A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296585.10:c.908A>G MANE Select	ENSP00000296585.5:p.Asn303Ser
ENST00000296585.9:c.908A>G	ENSP00000296585.5:p.Asn303Ser
ENST00000503810.6:c.*252A>G	ENSP00000426489.1:n.*252A>G
ENST00000509814.5:c.908A>G	ENSP00000424397.1:p.Asn303Ser
ENST00000509960.5:c.908A>G	ENSP00000424642.1:p.Asn303Ser
ENST00000510722.1:c.908A>G	ENSP00000422145.1:p.Asn303Ser
ENST00000513685.5:c.*622A>G	ENSP00000422095.1:n.*622A>G
NM_002203.3:c.908A>G	NP_002194.2:p.Asn303Ser
NR_073103.1:n.1051A>G
NR_073104.1:n.1051A>G
NR_073105.1:n.1051A>G
NR_073106.1:n.1051A>G
NR_073107.1:n.930A>G
NM_002203.4:c.908A>G MANE Select	NP_002194.2:p.Asn303Ser
NR_073103.2:n.1025A>G
NR_073104.2:n.1025A>G
NR_073105.2:n.1025A>G
NR_073106.2:n.1025A>G
NR_073107.2:n.904A>G