Canonical Allele Identifier: CA2396008583
Gene: GP1BB HGNC NCBI
SEPTIN5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.19724288G= , CM000684.2:g.19724288G= GRCh38
NC_000022.10:g.19711811G= , CM000684.1:g.19711811G= GRCh37
NC_000022.9:g.18091811G= NCBI36
NG_007974.1:g.5746G= , LRG_478:g.5746G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000366425.4:c.445G= (GP1BB) MANE Select ENSP00000383382.2:p.Gly149=
ENST00000366425.3:c.445G= (GP1BB) ENSP00000383382.2:p.Gly149=
ENST00000431044.5:c.*1530G= (SEPTIN5) ENSP00000399685.1:n.*1530G=
NM_000407.4:c.445G= , LRG_478t1:c.445G= (GP1BB) NP_000398.1:p.Gly149=
NR_037611.1:n.4185G=
NR_037612.1:n.2689G=
NM_000407.5:c.445G= (GP1BB) MANE Select NP_000398.1:p.Gly149=