Canonical Allele Identifier: CA2261365360

Gene: ITGA2B

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44374685_44374687delinsGCG , CM000679.2:g.44374685_44374687delinsGCG	GRCh38
NC_000017.10:g.42452053_42452055delinsGCG , CM000679.1:g.42452053_42452055delinsGCG	GRCh37
NC_000017.9:g.39807579_39807581delinsGCG	NCBI36
NG_008331.1:g.19819_19821delinsCGC , LRG_479:g.19819_19821delinsCGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262407.6:c.2915_2917delinsCGC MANE Select	ENSP00000262407.5:p.Pro972=
ENST00000648408.1:c.2346_2348delinsCGC
ENST00000262407.5:c.2915_2917delinsCGC	ENSP00000262407.5:p.Pro972=
ENST00000587295.5:c.253+1146_253+1148delinsCGC
ENST00000588098.1:c.9_11delinsCGC
ENST00000592462.5:n.2426_2428delinsCGC
NM_000419.3:c.2915_2917delinsCGC , LRG_479t1:c.2915_2917delinsCGC	NP_000410.2:p.Pro972=
XM_011524749.1:c.2842-217_2842-215delinsCGC	XP_011523051.1:n.2842-217_2842-215delinsCGC
XM_011524750.1:c.2915_2917delinsCGC	XP_011523052.1:p.Pro972=
NM_000419.4:c.2915_2917delinsCGC	NP_000410.2:p.Pro972=
NM_000419.5:c.2915_2917delinsCGC MANE Select	NP_000410.2:p.Pro972=