Canonical Allele Identifier: CA2396008712

Gene: GP1BB SEPTIN5

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19724482C= , CM000684.2:g.19724482C=	GRCh38
NC_000022.10:g.19712005C= , CM000684.1:g.19712005C=	GRCh37
NC_000022.9:g.18092005C=	NCBI36
NG_007974.1:g.5940C= , LRG_478:g.5940C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366425.4:c.*18C= (GP1BB) MANE Select	ENSP00000383382.2:n.*18C=
ENST00000366425.3:c.*18C= (GP1BB)	ENSP00000383382.2:n.*18C=
ENST00000431044.5:c.*1724C= (SEPTIN5)	ENSP00000399685.1:n.*1724C=
NM_000407.4:c.*18C= , LRG_478t1:c.*18C= (GP1BB)	NP_000398.1:n.*18C=
NR_037611.1:n.4379C=
NR_037612.1:n.2883C=
NM_000407.5:c.*18C= (GP1BB) MANE Select	NP_000398.1:n.*18C=