Canonical Allele Identifier: CA2963260862
Gene: ITGA2B HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44379792_44379793insCAA , CM000679.2:g.44379792_44379793insCAA GRCh38
NC_000017.10:g.42457160_42457161insCAA , CM000679.1:g.42457160_42457161insCAA GRCh37
NC_000017.9:g.39812686_39812687insCAA NCBI36
NG_008331.1:g.14713_14714insTTG , LRG_479:g.14713_14714insTTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000262407.6:c.1774_1775insTTG MANE Select ENSP00000262407.5:p.Lys592delinsIleGlu
ENST00000648408.1:c.1205_1206insTTG
ENST00000262407.5:c.1774_1775insTTG ENSP00000262407.5:p.Lys592delinsIleGlu
ENST00000592462.5:n.569_570insTTG
NM_000419.3:c.1774_1775insTTG , LRG_479t1:c.1774_1775insTTG NP_000410.2:p.Lys592delinsIleGlu
XM_011524749.1:c.1774_1775insTTG XP_011523051.1:p.Lys592delinsIleGlu
XM_011524750.1:c.1774_1775insTTG XP_011523052.1:p.Lys592delinsIleGlu
NM_000419.4:c.1774_1775insTTG NP_000410.2:p.Lys592delinsIleGlu
NM_000419.5:c.1774_1775insTTG MANE Select NP_000410.2:p.Lys592delinsIleGlu
Search 100 bp 5'
Search 100 bp 3'