Canonical Allele Identifier: CA2396008663

Gene: GP1BB SEPTIN5

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19724422C= , CM000684.2:g.19724422C=	GRCh38
NC_000022.10:g.19711945C= , CM000684.1:g.19711945C=	GRCh37
NC_000022.9:g.18091945C=	NCBI36
NG_007974.1:g.5880C= , LRG_478:g.5880C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366425.4:c.579C= (GP1BB) MANE Select	ENSP00000383382.2:p.Thr193=
ENST00000366425.3:c.579C= (GP1BB)	ENSP00000383382.2:p.Thr193=
ENST00000431044.5:c.*1664C= (SEPTIN5)	ENSP00000399685.1:n.*1664C=
NM_000407.4:c.579C= , LRG_478t1:c.579C= (GP1BB)	NP_000398.1:p.Thr193=
NR_037611.1:n.4319C=
NR_037612.1:n.2823C=
NM_000407.5:c.579C= (GP1BB) MANE Select	NP_000398.1:p.Thr193=