Canonical Allele Identifier: CA2396008657

Gene: GP1BB SEPTIN5

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19724409G= , CM000684.2:g.19724409G=	GRCh38
NC_000022.10:g.19711932G= , CM000684.1:g.19711932G=	GRCh37
NC_000022.9:g.18091932G=	NCBI36
NG_007974.1:g.5867G= , LRG_478:g.5867G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366425.4:c.566G= (GP1BB) MANE Select	ENSP00000383382.2:p.Arg189=
ENST00000366425.3:c.566G= (GP1BB)	ENSP00000383382.2:p.Arg189=
ENST00000431044.5:c.*1651G= (SEPTIN5)	ENSP00000399685.1:n.*1651G=
NM_000407.4:c.566G= , LRG_478t1:c.566G= (GP1BB)	NP_000398.1:p.Arg189=
NR_037611.1:n.4306G=
NR_037612.1:n.2810G=
NM_000407.5:c.566G= (GP1BB) MANE Select	NP_000398.1:p.Arg189=