Canonical Allele Identifier: CA2655305321
Gene: GP1BB HGNC NCBI
SEPTIN5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.19724090_19724146del , CM000684.2:g.19724090_19724146del GRCh38
NC_000022.10:g.19711613_19711669del , CM000684.1:g.19711613_19711669del GRCh37
NC_000022.9:g.18091613_18091669del NCBI36
NG_007974.1:g.5548_5604del , LRG_478:g.5548_5604del

Transcript Alleles

HGVS Amino-acid change
ENST00000366425.4:c.247_303del (GP1BB) MANE Select ENSP00000383382.2:p.Thr83_Arg101del
ENST00000366425.3:c.247_303del (GP1BB) ENSP00000383382.2:p.Thr83_Arg101del
ENST00000431044.5:c.*1332_*1388del (SEPTIN5) ENSP00000399685.1:n.*1332_*1388del
ENST00000455843.5:c.*1332_*1388del (SEPTIN5) ENSP00000391731.1:n.*1332_*1388del
ENST00000470814.1:n.2219_2275del (SEPTIN5)
NM_000407.4:c.247_303del , LRG_478t1:c.247_303del (GP1BB) NP_000398.1:p.Thr83_Arg101del
NR_037611.1:n.3987_4043del
NR_037612.1:n.2491_2547del
NM_000407.5:c.247_303del (GP1BB) MANE Select NP_000398.1:p.Thr83_Arg101del