Canonical Allele Identifier: CA2655305185

Gene: GP1BB SEPTIN5

Linked Data

• gnomAD v4: 22-19723878-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19723879del , CM000684.2:g.19723879del	GRCh38
NC_000022.10:g.19711402del , CM000684.1:g.19711402del	GRCh37
NC_000022.9:g.18091402del	NCBI36
NG_007974.1:g.5337del , LRG_478:g.5337del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366425.4:c.36del (GP1BB) MANE Select	ENSP00000383382.2:p.Leu13SerfsTer?
ENST00000366425.3:c.36del (GP1BB)	ENSP00000383382.2:p.Leu13SerfsTer?
ENST00000431044.5:c.*1121del (SEPTIN5)	ENSP00000399685.1:n.*1121del
ENST00000455843.5:c.*1121del (SEPTIN5)	ENSP00000391731.1:n.*1121del
ENST00000470814.1:n.2008del (SEPTIN5)
NM_000407.4:c.36del , LRG_478t1:c.36del (GP1BB)	NP_000398.1:p.Leu13SerfsTer?
NR_037611.1:n.3776del
NR_037612.1:n.2280del
NM_000407.5:c.36del (GP1BB) MANE Select	NP_000398.1:p.Leu13SerfsTer?