Canonical Allele Identifier: CA444163392

Gene: ITGA2

Linked Data

• MyVariant Identifiers: chr5:g.52351455T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.53055625T>C , CM000667.2:g.53055625T>C	GRCh38
NC_000005.9:g.52351455T>C , CM000667.1:g.52351455T>C	GRCh37
NC_000005.8:g.52387212T>C	NCBI36
NG_008330.1:g.71300T>C
NG_008330.2:g.71300T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296585.10:c.867T>C MANE Select	ENSP00000296585.5:p.Gly289=
ENST00000296585.9:c.867T>C	ENSP00000296585.5:p.Gly289=
ENST00000503810.6:c.*211T>C	ENSP00000426489.1:n.*211T>C
ENST00000509814.5:c.867T>C	ENSP00000424397.1:p.Gly289=
ENST00000509960.5:c.867T>C	ENSP00000424642.1:p.Gly289=
ENST00000510722.1:c.867T>C	ENSP00000422145.1:p.Gly289=
ENST00000513685.5:c.*581T>C	ENSP00000422095.1:n.*581T>C
NM_002203.3:c.867T>C	NP_002194.2:p.Gly289=
NR_073103.1:n.1010T>C
NR_073104.1:n.1010T>C
NR_073105.1:n.1010T>C
NR_073106.1:n.1010T>C
NR_073107.1:n.889T>C
NM_002203.4:c.867T>C MANE Select	NP_002194.2:p.Gly289=
NR_073103.2:n.984T>C
NR_073104.2:n.984T>C
NR_073105.2:n.984T>C
NR_073106.2:n.984T>C
NR_073107.2:n.863T>C