Canonical Allele Identifier: CA2655304974

Gene: GP1BB SEPTIN5

Linked Data

• gnomAD v4: 22-19723824-GCTC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19723825_19723827del , CM000684.2:g.19723825_19723827del	GRCh38
NC_000022.10:g.19711348_19711350del , CM000684.1:g.19711348_19711350del	GRCh37
NC_000022.9:g.18091348_18091350del	NCBI36
NG_007974.1:g.5283_5285del , LRG_478:g.5283_5285del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366425.4:c.11-29_11-27del (GP1BB) MANE Select	ENSP00000383382.2:n.11-29_11-27del
ENST00000366425.3:c.11-29_11-27del (GP1BB)	ENSP00000383382.2:n.11-29_11-27del
ENST00000431044.5:c.*1096-29_*1096-27del (SEPTIN5)	ENSP00000399685.1:n.*1096-29_*1096-27del
ENST00000455843.5:c.*1096-29_*1096-27del (SEPTIN5)	ENSP00000391731.1:n.*1096-29_*1096-27del
ENST00000470814.1:n.1983-29_1983-27del (SEPTIN5)
NM_000407.4:c.11-29_11-27del , LRG_478t1:c.11-29_11-27del (GP1BB)	NP_000398.1:n.11-29_11-27del
NR_037611.1:n.3751-29_3751-27del
NR_037612.1:n.2255-29_2255-27del
NM_000407.5:c.11-29_11-27del (GP1BB) MANE Select	NP_000398.1:n.11-29_11-27del