Canonical Allele Identifier: CA2396008329

Gene: GP1BB SEPTIN5

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19723807C= , CM000684.2:g.19723807C=	GRCh38
NC_000022.10:g.19711330C= , CM000684.1:g.19711330C=	GRCh37
NC_000022.9:g.18091330C=	NCBI36
NG_007974.1:g.5265C= , LRG_478:g.5265C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366425.4:c.11-47C= (GP1BB) MANE Select	ENSP00000383382.2:n.11-47C=
ENST00000366425.3:c.11-47C= (GP1BB)	ENSP00000383382.2:n.11-47C=
ENST00000431044.5:c.*1096-47C= (SEPTIN5)	ENSP00000399685.1:n.*1096-47C=
ENST00000455843.5:c.*1096-47C= (SEPTIN5)	ENSP00000391731.1:n.*1096-47C=
ENST00000470814.1:n.1983-47C= (SEPTIN5)
NM_000407.4:c.11-47C= , LRG_478t1:c.11-47C= (GP1BB)	NP_000398.1:n.11-47C=
NR_037611.1:n.3751-47C=
NR_037612.1:n.2255-47C=
NM_000407.5:c.11-47C= (GP1BB) MANE Select	NP_000398.1:n.11-47C=