Canonical Allele Identifier: CA1024129218
Gene: GP1BB HGNC NCBI
SEPTIN5 HGNC NCBI

Linked Data

dbSNP Id: rs1936116289

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.19724154_19724157dup , CM000684.2:g.19724154_19724157dup GRCh38
NC_000022.10:g.19711677_19711680dup , CM000684.1:g.19711677_19711680dup GRCh37
NC_000022.9:g.18091677_18091680dup NCBI36
NG_007974.1:g.5612_5615dup , LRG_478:g.5612_5615dup

Transcript Alleles

HGVS Amino-acid change
ENST00000366425.4:c.311_314dup (GP1BB) MANE Select ENSP00000383382.2:p.Glu109ProfsTer?
ENST00000366425.3:c.311_314dup (GP1BB) ENSP00000383382.2:p.Glu109ProfsTer?
ENST00000431044.5:c.*1396_*1399dup (SEPTIN5) ENSP00000399685.1:n.*1396_*1399dup
ENST00000455843.5:c.*1396_*1399dup (SEPTIN5) ENSP00000391731.1:n.*1396_*1399dup
ENST00000470814.1:n.2283_2286dup (SEPTIN5)
NM_000407.4:c.311_314dup , LRG_478t1:c.311_314dup (GP1BB) NP_000398.1:p.Glu109ProfsTer?
NR_037611.1:n.4051_4054dup
NR_037612.1:n.2555_2558dup
NM_000407.5:c.311_314dup (GP1BB) MANE Select NP_000398.1:p.Glu109ProfsTer?