Canonical Allele Identifier: CA2261365700

Gene: ITGA2B

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44375317_44375318delinsTC , CM000679.2:g.44375317_44375318delinsTC	GRCh38
NC_000017.10:g.42452685_42452686delinsTC , CM000679.1:g.42452685_42452686delinsTC	GRCh37
NC_000017.9:g.39808211_39808212delinsTC	NCBI36
NG_008331.1:g.19188_19189delinsGA , LRG_479:g.19188_19189delinsGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262407.6:c.2728-207_2728-206delinsGA MANE Select	ENSP00000262407.5:n.2728-207_2728-206delinsGA
ENST00000648408.1:c.2159-207_2159-206delinsGA
ENST00000262407.5:c.2728-207_2728-206delinsGA	ENSP00000262407.5:n.2728-207_2728-206delinsGA
ENST00000587295.5:c.253+515_253+516delinsGA
ENST00000592462.5:n.1795_1796delinsGA
NM_000419.3:c.2728-207_2728-206delinsGA , LRG_479t1:c.2728-207_2728-206delinsGA	NP_000410.2:n.2728-207_2728-206delinsGA
XM_011524749.1:c.2728-207_2728-206delinsGA	XP_011523051.1:n.2728-207_2728-206delinsGA
XM_011524750.1:c.2728-207_2728-206delinsGA	XP_011523052.1:n.2728-207_2728-206delinsGA
NM_000419.4:c.2728-207_2728-206delinsGA	NP_000410.2:n.2728-207_2728-206delinsGA
NM_000419.5:c.2728-207_2728-206delinsGA MANE Select	NP_000410.2:n.2728-207_2728-206delinsGA