Canonical Allele Identifier: CA2396008698

Gene: GP1BB SEPTIN5

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19724470G= , CM000684.2:g.19724470G=	GRCh38
NC_000022.10:g.19711993G= , CM000684.1:g.19711993G=	GRCh37
NC_000022.9:g.18091993G=	NCBI36
NG_007974.1:g.5928G= , LRG_478:g.5928G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366425.4:c.*6G= (GP1BB) MANE Select	ENSP00000383382.2:n.*6G=
ENST00000366425.3:c.*6G= (GP1BB)	ENSP00000383382.2:n.*6G=
ENST00000431044.5:c.*1712G= (SEPTIN5)	ENSP00000399685.1:n.*1712G=
NM_000407.4:c.*6G= , LRG_478t1:c.*6G= (GP1BB)	NP_000398.1:n.*6G=
NR_037611.1:n.4367G=
NR_037612.1:n.2871G=
NM_000407.5:c.*6G= (GP1BB) MANE Select	NP_000398.1:n.*6G=