Canonical Allele Identifier: CA1024129168

Gene: GP1BB SEPTIN5

Linked Data

• dbSNP Id: rs1936108270
• gnomAD v3: 22-19723846-C-G
• gnomAD v4: 22-19723846-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19723846C>G , CM000684.2:g.19723846C>G	GRCh38
NC_000022.10:g.19711369C>G , CM000684.1:g.19711369C>G	GRCh37
NC_000022.9:g.18091369C>G	NCBI36
NG_007974.1:g.5304C>G , LRG_478:g.5304C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366425.4:c.11-8C>G (GP1BB) MANE Select	ENSP00000383382.2:n.11-8C>G
ENST00000366425.3:c.11-8C>G (GP1BB)	ENSP00000383382.2:n.11-8C>G
ENST00000431044.5:c.*1096-8C>G (SEPTIN5)	ENSP00000399685.1:n.*1096-8C>G
ENST00000455843.5:c.*1096-8C>G (SEPTIN5)	ENSP00000391731.1:n.*1096-8C>G
ENST00000470814.1:n.1983-8C>G (SEPTIN5)
NM_000407.4:c.11-8C>G , LRG_478t1:c.11-8C>G (GP1BB)	NP_000398.1:n.11-8C>G
NR_037611.1:n.3751-8C>G
NR_037612.1:n.2255-8C>G
NM_000407.5:c.11-8C>G (GP1BB) MANE Select	NP_000398.1:n.11-8C>G