Canonical Allele Identifier: CA410677288
Gene: GP1BB HGNC NCBI
SEPTIN5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.19724210G>A , CM000684.2:g.19724210G>A GRCh38
NC_000022.10:g.19711733G>A , CM000684.1:g.19711733G>A GRCh37
NC_000022.9:g.18091733G>A NCBI36
NG_007974.1:g.5668G>A , LRG_478:g.5668G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000366425.4:c.367G>A (GP1BB) MANE Select ENSP00000383382.2:p.Ala123Thr
ENST00000366425.3:c.367G>A (GP1BB) ENSP00000383382.2:p.Ala123Thr
ENST00000431044.5:c.*1452G>A (SEPTIN5) ENSP00000399685.1:n.*1452G>A
ENST00000455843.5:c.*1452G>A (SEPTIN5) ENSP00000391731.1:n.*1452G>A
ENST00000470814.1:n.2339G>A (SEPTIN5)
NM_000407.4:c.367G>A , LRG_478t1:c.367G>A (GP1BB) NP_000398.1:p.Ala123Thr
NR_037611.1:n.4107G>A
NR_037612.1:n.2611G>A
NM_000407.5:c.367G>A (GP1BB) MANE Select NP_000398.1:p.Ala123Thr