Canonical Allele Identifier: CA410677079
Gene: GP1BB HGNC NCBI
SEPTIN5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.19724150T>A , CM000684.2:g.19724150T>A GRCh38
NC_000022.10:g.19711673T>A , CM000684.1:g.19711673T>A GRCh37
NC_000022.9:g.18091673T>A NCBI36
NG_007974.1:g.5608T>A , LRG_478:g.5608T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000366425.4:c.307T>A (GP1BB) MANE Select ENSP00000383382.2:p.Trp103Arg
ENST00000366425.3:c.307T>A (GP1BB) ENSP00000383382.2:p.Trp103Arg
ENST00000431044.5:c.*1392T>A (SEPTIN5) ENSP00000399685.1:n.*1392T>A
ENST00000455843.5:c.*1392T>A (SEPTIN5) ENSP00000391731.1:n.*1392T>A
ENST00000470814.1:n.2279T>A (SEPTIN5)
NM_000407.4:c.307T>A , LRG_478t1:c.307T>A (GP1BB) NP_000398.1:p.Trp103Arg
NR_037611.1:n.4047T>A
NR_037612.1:n.2551T>A
NM_000407.5:c.307T>A (GP1BB) MANE Select NP_000398.1:p.Trp103Arg