Canonical Allele Identifier: CA2396008362

Gene: GP1BB SEPTIN5

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19723862G= , CM000684.2:g.19723862G=	GRCh38
NC_000022.10:g.19711385G= , CM000684.1:g.19711385G=	GRCh37
NC_000022.9:g.18091385G=	NCBI36
NG_007974.1:g.5320G= , LRG_478:g.5320G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366425.4:c.19G= (GP1BB) MANE Select	ENSP00000383382.2:p.Gly7=
ENST00000366425.3:c.19G= (GP1BB)	ENSP00000383382.2:p.Gly7=
ENST00000431044.5:c.*1104G= (SEPTIN5)	ENSP00000399685.1:n.*1104G=
ENST00000455843.5:c.*1104G= (SEPTIN5)	ENSP00000391731.1:n.*1104G=
ENST00000470814.1:n.1991G= (SEPTIN5)
NM_000407.4:c.19G= , LRG_478t1:c.19G= (GP1BB)	NP_000398.1:p.Gly7=
NR_037611.1:n.3759G=
NR_037612.1:n.2263G=
NM_000407.5:c.19G= (GP1BB) MANE Select	NP_000398.1:p.Gly7=