Canonical Allele Identifier: CA2396008677

Gene: GP1BB SEPTIN5

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19724443A= , CM000684.2:g.19724443A=	GRCh38
NC_000022.10:g.19711966A= , CM000684.1:g.19711966A=	GRCh37
NC_000022.9:g.18091966A=	NCBI36
NG_007974.1:g.5901A= , LRG_478:g.5901A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366425.4:c.600A= (GP1BB) MANE Select	ENSP00000383382.2:p.Arg200=
ENST00000366425.3:c.600A= (GP1BB)	ENSP00000383382.2:p.Arg200=
ENST00000431044.5:c.*1685A= (SEPTIN5)	ENSP00000399685.1:n.*1685A=
NM_000407.4:c.600A= , LRG_478t1:c.600A= (GP1BB)	NP_000398.1:p.Arg200=
NR_037611.1:n.4340A=
NR_037612.1:n.2844A=
NM_000407.5:c.600A= (GP1BB) MANE Select	NP_000398.1:p.Arg200=