Canonical Allele Identifier: CA2396008498
Gene: GP1BB HGNC NCBI
SEPTIN5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.19724148C= , CM000684.2:g.19724148C= GRCh38
NC_000022.10:g.19711671C= , CM000684.1:g.19711671C= GRCh37
NC_000022.9:g.18091671C= NCBI36
NG_007974.1:g.5606C= , LRG_478:g.5606C=

Transcript Alleles

HGVS Amino-acid change
ENST00000366425.4:c.305C= (GP1BB) MANE Select ENSP00000383382.2:p.Ala102=
ENST00000366425.3:c.305C= (GP1BB) ENSP00000383382.2:p.Ala102=
ENST00000431044.5:c.*1390C= (SEPTIN5) ENSP00000399685.1:n.*1390C=
ENST00000455843.5:c.*1390C= (SEPTIN5) ENSP00000391731.1:n.*1390C=
ENST00000470814.1:n.2277C= (SEPTIN5)
NM_000407.4:c.305C= , LRG_478t1:c.305C= (GP1BB) NP_000398.1:p.Ala102=
NR_037611.1:n.4045C=
NR_037612.1:n.2549C=
NM_000407.5:c.305C= (GP1BB) MANE Select NP_000398.1:p.Ala102=