Canonical Allele Identifier: CA410677402
Gene: GP1BB HGNC NCBI
SEPTIN5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.19724244A>C , CM000684.2:g.19724244A>C GRCh38
NC_000022.10:g.19711767A>C , CM000684.1:g.19711767A>C GRCh37
NC_000022.9:g.18091767A>C NCBI36
NG_007974.1:g.5702A>C , LRG_478:g.5702A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000366425.4:c.401A>C (GP1BB) MANE Select ENSP00000383382.2:p.Glu134Ala
ENST00000366425.3:c.401A>C (GP1BB) ENSP00000383382.2:p.Glu134Ala
ENST00000431044.5:c.*1486A>C (SEPTIN5) ENSP00000399685.1:n.*1486A>C
NM_000407.4:c.401A>C , LRG_478t1:c.401A>C (GP1BB) NP_000398.1:p.Glu134Ala
NR_037611.1:n.4141A>C
NR_037612.1:n.2645A>C
NM_000407.5:c.401A>C (GP1BB) MANE Select NP_000398.1:p.Glu134Ala