Canonical Allele Identifier: CA2396008587
Gene: GP1BB HGNC NCBI
SEPTIN5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.19724293G= , CM000684.2:g.19724293G= GRCh38
NC_000022.10:g.19711816G= , CM000684.1:g.19711816G= GRCh37
NC_000022.9:g.18091816G= NCBI36
NG_007974.1:g.5751G= , LRG_478:g.5751G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000366425.4:c.450G= (GP1BB) MANE Select ENSP00000383382.2:p.Ala150=
ENST00000366425.3:c.450G= (GP1BB) ENSP00000383382.2:p.Ala150=
ENST00000431044.5:c.*1535G= (SEPTIN5) ENSP00000399685.1:n.*1535G=
NM_000407.4:c.450G= , LRG_478t1:c.450G= (GP1BB) NP_000398.1:p.Ala150=
NR_037611.1:n.4190G=
NR_037612.1:n.2694G=
NM_000407.5:c.450G= (GP1BB) MANE Select NP_000398.1:p.Ala150=