Canonical Allele Identifier: CA2839075721

Gene: ITGA2B

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44374940_44374943del , CM000679.2:g.44374940_44374943del	GRCh38
NC_000017.10:g.42452308_42452311del , CM000679.1:g.42452308_42452311del	GRCh37
NC_000017.9:g.39807834_39807837del	NCBI36
NG_008331.1:g.19563_19566del , LRG_479:g.19563_19566del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262407.6:c.2841+55_2841+58del MANE Select	ENSP00000262407.5:n.2841+55_2841+58del
ENST00000648408.1:c.2272+55_2272+58del
ENST00000262407.5:c.2841+55_2841+58del	ENSP00000262407.5:n.2841+55_2841+58del
ENST00000587295.5:c.253+890_253+893del
ENST00000592462.5:n.2170_2173del
NM_000419.3:c.2841+55_2841+58del , LRG_479t1:c.2841+55_2841+58del	NP_000410.2:n.2841+55_2841+58del
XM_011524749.1:c.2841+55_2841+58del	XP_011523051.1:n.2841+55_2841+58del
XM_011524750.1:c.2841+55_2841+58del	XP_011523052.1:n.2841+55_2841+58del
NM_000419.4:c.2841+55_2841+58del	NP_000410.2:n.2841+55_2841+58del
NM_000419.5:c.2841+55_2841+58del MANE Select	NP_000410.2:n.2841+55_2841+58del