Canonical Allele Identifier: CA2396008588
Gene: GP1BB HGNC NCBI
SEPTIN5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.19724294C= , CM000684.2:g.19724294C= GRCh38
NC_000022.10:g.19711817C= , CM000684.1:g.19711817C= GRCh37
NC_000022.9:g.18091817C= NCBI36
NG_007974.1:g.5752C= , LRG_478:g.5752C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000366425.4:c.451C= (GP1BB) MANE Select ENSP00000383382.2:p.Leu151=
ENST00000366425.3:c.451C= (GP1BB) ENSP00000383382.2:p.Leu151=
ENST00000431044.5:c.*1536C= (SEPTIN5) ENSP00000399685.1:n.*1536C=
NM_000407.4:c.451C= , LRG_478t1:c.451C= (GP1BB) NP_000398.1:p.Leu151=
NR_037611.1:n.4191C=
NR_037612.1:n.2695C=
NM_000407.5:c.451C= (GP1BB) MANE Select NP_000398.1:p.Leu151=