Canonical Allele Identifier: CA2739747083

Gene: GP1BB SEPTIN5

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19723820G>C , CM000684.2:g.19723820G>C	GRCh38
NC_000022.10:g.19711343G>C , CM000684.1:g.19711343G>C	GRCh37
NC_000022.9:g.18091343G>C	NCBI36
NG_007974.1:g.5278G>C , LRG_478:g.5278G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366425.4:c.11-34G>C (GP1BB) MANE Select	ENSP00000383382.2:n.11-34G>C
ENST00000366425.3:c.11-34G>C (GP1BB)	ENSP00000383382.2:n.11-34G>C
ENST00000431044.5:c.*1096-34G>C (SEPTIN5)	ENSP00000399685.1:n.*1096-34G>C
ENST00000455843.5:c.*1096-34G>C (SEPTIN5)	ENSP00000391731.1:n.*1096-34G>C
ENST00000470814.1:n.1983-34G>C (SEPTIN5)
NM_000407.4:c.11-34G>C , LRG_478t1:c.11-34G>C (GP1BB)	NP_000398.1:n.11-34G>C
NR_037611.1:n.3751-34G>C
NR_037612.1:n.2255-34G>C
NM_000407.5:c.11-34G>C (GP1BB) MANE Select	NP_000398.1:n.11-34G>C