Canonical Allele Identifier: CA359684523

Gene: ITGA2

Linked Data

• gnomAD v4: 5-53055624-G-A
• MyVariant Identifiers: chr5:g.52351454G>A (hg19) ; chr5:g.53055624G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.53055624G>A , CM000667.2:g.53055624G>A	GRCh38
NC_000005.9:g.52351454G>A , CM000667.1:g.52351454G>A	GRCh37
NC_000005.8:g.52387211G>A	NCBI36
NG_008330.1:g.71299G>A
NG_008330.2:g.71299G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296585.10:c.866G>A MANE Select	ENSP00000296585.5:p.Gly289Asp
ENST00000296585.9:c.866G>A	ENSP00000296585.5:p.Gly289Asp
ENST00000503810.6:c.*210G>A	ENSP00000426489.1:n.*210G>A
ENST00000509814.5:c.866G>A	ENSP00000424397.1:p.Gly289Asp
ENST00000509960.5:c.866G>A	ENSP00000424642.1:p.Gly289Asp
ENST00000510722.1:c.866G>A	ENSP00000422145.1:p.Gly289Asp
ENST00000513685.5:c.*580G>A	ENSP00000422095.1:n.*580G>A
NM_002203.3:c.866G>A	NP_002194.2:p.Gly289Asp
NR_073103.1:n.1009G>A
NR_073104.1:n.1009G>A
NR_073105.1:n.1009G>A
NR_073106.1:n.1009G>A
NR_073107.1:n.888G>A
NM_002203.4:c.866G>A MANE Select	NP_002194.2:p.Gly289Asp
NR_073103.2:n.983G>A
NR_073104.2:n.983G>A
NR_073105.2:n.983G>A
NR_073106.2:n.983G>A
NR_073107.2:n.862G>A