Canonical Allele Identifier: CA410676327
Gene: GP1BB HGNC NCBI
SEPTIN5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.19723916G>T , CM000684.2:g.19723916G>T GRCh38
NC_000022.10:g.19711439G>T , CM000684.1:g.19711439G>T GRCh37
NC_000022.9:g.18091439G>T NCBI36
NG_007974.1:g.5374G>T , LRG_478:g.5374G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000366425.4:c.73G>T (GP1BB) MANE Select ENSP00000383382.2:p.Gly25Cys
ENST00000366425.3:c.73G>T (GP1BB) ENSP00000383382.2:p.Gly25Cys
ENST00000431044.5:c.*1158G>T (SEPTIN5) ENSP00000399685.1:n.*1158G>T
ENST00000455843.5:c.*1158G>T (SEPTIN5) ENSP00000391731.1:n.*1158G>T
ENST00000470814.1:n.2045G>T (SEPTIN5)
NM_000407.4:c.73G>T , LRG_478t1:c.73G>T (GP1BB) NP_000398.1:p.Gly25Cys
NR_037611.1:n.3813G>T
NR_037612.1:n.2317G>T
NM_000407.5:c.73G>T (GP1BB) MANE Select NP_000398.1:p.Gly25Cys