Canonical Allele Identifier: CA2262604913
Gene: ITGB3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.47283564_47283566delinsCTT , CM000679.2:g.47283564_47283566delinsCTT GRCh38
NC_000017.10:g.45360930_45360932delinsCTT , CM000679.1:g.45360930_45360932delinsCTT GRCh37
NC_000017.9:g.42715929_42715931delinsCTT NCBI36
NG_008332.2:g.34723_34725delinsCTT , LRG_481:g.34723_34725delinsCTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000696963.1:c.361+15_361+17delinsCTT ENSP00000513002.1:n.361+15_361+17delinsCTT
ENST00000559488.7:c.361+15_361+17delinsCTT MANE Select ENSP00000452786.2:n.361+15_361+17delinsCTT
ENST00000559488.5:c.361+15_361+17delinsCTT ENSP00000452786.1:n.361+15_361+17delinsCTT
ENST00000560629.1:c.326+15_326+17delinsCTT
ENST00000571680.1:c.361+15_361+17delinsCTT ENSP00000461626.1:n.361+15_361+17delinsCTT
NM_000212.2:c.361+15_361+17delinsCTT , LRG_481t1:c.361+15_361+17delinsCTT NP_000203.2:n.361+15_361+17delinsCTT
NM_000212.3:c.361+15_361+17delinsCTT MANE Select NP_000203.2:n.361+15_361+17delinsCTT