Canonical Allele Identifier: CA2396008679

Gene: GP1BB SEPTIN5

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19724446C= , CM000684.2:g.19724446C=	GRCh38
NC_000022.10:g.19711969C= , CM000684.1:g.19711969C=	GRCh37
NC_000022.9:g.18091969C=	NCBI36
NG_007974.1:g.5904C= , LRG_478:g.5904C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366425.4:c.603C= (GP1BB) MANE Select	ENSP00000383382.2:p.Ala201=
ENST00000366425.3:c.603C= (GP1BB)	ENSP00000383382.2:p.Ala201=
ENST00000431044.5:c.*1688C= (SEPTIN5)	ENSP00000399685.1:n.*1688C=
NM_000407.4:c.603C= , LRG_478t1:c.603C= (GP1BB)	NP_000398.1:p.Ala201=
NR_037611.1:n.4343C=
NR_037612.1:n.2847C=
NM_000407.5:c.603C= (GP1BB) MANE Select	NP_000398.1:p.Ala201=