Canonical Allele Identifier: CA2655305399
Gene: GP1BB HGNC NCBI
SEPTIN5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.19724260_19724303del , CM000684.2:g.19724260_19724303del GRCh38
NC_000022.10:g.19711783_19711826del , CM000684.1:g.19711783_19711826del GRCh37
NC_000022.9:g.18091783_18091826del NCBI36
NG_007974.1:g.5718_5761del , LRG_478:g.5718_5761del

Transcript Alleles

HGVS Amino-acid Change
ENST00000366425.4:c.417_460del (GP1BB) MANE Select ENSP00000383382.2:p.Pro143AlafsTer?
ENST00000366425.3:c.417_460del (GP1BB) ENSP00000383382.2:p.Pro143AlafsTer?
ENST00000431044.5:c.*1502_*1545del (SEPTIN5) ENSP00000399685.1:n.*1502_*1545del
NM_000407.4:c.417_460del , LRG_478t1:c.417_460del (GP1BB) NP_000398.1:p.Pro143AlafsTer?
NR_037611.1:n.4157_4200del
NR_037612.1:n.2661_2704del
NM_000407.5:c.417_460del (GP1BB) MANE Select NP_000398.1:p.Pro143AlafsTer?