Canonical Allele Identifier: CA2837995121

Gene: ITGA2B

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44372391_44372392insCA , CM000679.2:g.44372391_44372392insCA	GRCh38
NC_000017.10:g.42449759_42449760insCA , CM000679.1:g.42449759_42449760insCA	GRCh37
NC_000017.9:g.39805285_39805286insCA	NCBI36
NG_008331.1:g.22114_22115insTG , LRG_479:g.22114_22115insTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262407.6:c.3092_3093insTG MANE Select	ENSP00000262407.5:p.Glu1032GlyfsTer?
ENST00000648408.1:c.2406_2407insTG
ENST00000262407.5:c.3092_3093insTG	ENSP00000262407.5:p.Glu1032GlyfsTer?
ENST00000587295.5:c.285_286insTG
ENST00000588098.1:c.69_70insTG
NM_000419.3:c.3092_3093insTG , LRG_479t1:c.3092_3093insTG	NP_000410.2:p.Glu1032GlyfsTer?
XM_011524749.1:c.2990_2991insTG	XP_011523051.1:p.Glu998GlyfsTer?
XM_011524750.1:c.2975_2976insTG	XP_011523052.1:p.Glu993GlyfsTer?
NM_000419.4:c.3092_3093insTG	NP_000410.2:p.Glu1032GlyfsTer?
NM_000419.5:c.3092_3093insTG MANE Select	NP_000410.2:p.Glu1032GlyfsTer?