Canonical Allele Identifier: CA2396008562
Gene: GP1BB HGNC NCBI
SEPTIN5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.19724260C= , CM000684.2:g.19724260C= GRCh38
NC_000022.10:g.19711783C= , CM000684.1:g.19711783C= GRCh37
NC_000022.9:g.18091783C= NCBI36
NG_007974.1:g.5718C= , LRG_478:g.5718C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000366425.4:c.417C= (GP1BB) MANE Select ENSP00000383382.2:p.Ala139=
ENST00000366425.3:c.417C= (GP1BB) ENSP00000383382.2:p.Ala139=
ENST00000431044.5:c.*1502C= (SEPTIN5) ENSP00000399685.1:n.*1502C=
NM_000407.4:c.417C= , LRG_478t1:c.417C= (GP1BB) NP_000398.1:p.Ala139=
NR_037611.1:n.4157C=
NR_037612.1:n.2661C=
NM_000407.5:c.417C= (GP1BB) MANE Select NP_000398.1:p.Ala139=