Canonical Allele Identifier: CA2396008610
Gene: GP1BB HGNC NCBI
SEPTIN5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.19724340T= , CM000684.2:g.19724340T= GRCh38
NC_000022.10:g.19711863T= , CM000684.1:g.19711863T= GRCh37
NC_000022.9:g.18091863T= NCBI36
NG_007974.1:g.5798T= , LRG_478:g.5798T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000366425.4:c.497T= (GP1BB) MANE Select ENSP00000383382.2:p.Leu166=
ENST00000366425.3:c.497T= (GP1BB) ENSP00000383382.2:p.Leu166=
ENST00000431044.5:c.*1582T= (SEPTIN5) ENSP00000399685.1:n.*1582T=
NM_000407.4:c.497T= , LRG_478t1:c.497T= (GP1BB) NP_000398.1:p.Leu166=
NR_037611.1:n.4237T=
NR_037612.1:n.2741T=
NM_000407.5:c.497T= (GP1BB) MANE Select NP_000398.1:p.Leu166=