Canonical Allele Identifier: CA2396008661

Gene: GP1BB SEPTIN5

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19724419G= , CM000684.2:g.19724419G=	GRCh38
NC_000022.10:g.19711942G= , CM000684.1:g.19711942G=	GRCh37
NC_000022.9:g.18091942G=	NCBI36
NG_007974.1:g.5877G= , LRG_478:g.5877G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366425.4:c.576G= (GP1BB) MANE Select	ENSP00000383382.2:p.Leu192=
ENST00000366425.3:c.576G= (GP1BB)	ENSP00000383382.2:p.Leu192=
ENST00000431044.5:c.*1661G= (SEPTIN5)	ENSP00000399685.1:n.*1661G=
NM_000407.4:c.576G= , LRG_478t1:c.576G= (GP1BB)	NP_000398.1:p.Leu192=
NR_037611.1:n.4316G=
NR_037612.1:n.2820G=
NM_000407.5:c.576G= (GP1BB) MANE Select	NP_000398.1:p.Leu192=