Canonical Allele Identifier: CA2396008413

Gene: GP1BB SEPTIN5

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19723964C= , CM000684.2:g.19723964C=	GRCh38
NC_000022.10:g.19711487C= , CM000684.1:g.19711487C=	GRCh37
NC_000022.9:g.18091487C=	NCBI36
NG_007974.1:g.5422C= , LRG_478:g.5422C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366425.4:c.121C= (GP1BB) MANE Select	ENSP00000383382.2:p.Arg41=
ENST00000366425.3:c.121C= (GP1BB)	ENSP00000383382.2:p.Arg41=
ENST00000431044.5:c.*1206C= (SEPTIN5)	ENSP00000399685.1:n.*1206C=
ENST00000455843.5:c.*1206C= (SEPTIN5)	ENSP00000391731.1:n.*1206C=
ENST00000470814.1:n.2093C= (SEPTIN5)
NM_000407.4:c.121C= , LRG_478t1:c.121C= (GP1BB)	NP_000398.1:p.Arg41=
NR_037611.1:n.3861C=
NR_037612.1:n.2365C=
NM_000407.5:c.121C= (GP1BB) MANE Select	NP_000398.1:p.Arg41=