Canonical Allele Identifier: CA2396008624
Gene: GP1BB HGNC NCBI
SEPTIN5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.19724372A= , CM000684.2:g.19724372A= GRCh38
NC_000022.10:g.19711895A= , CM000684.1:g.19711895A= GRCh37
NC_000022.9:g.18091895A= NCBI36
NG_007974.1:g.5830A= , LRG_478:g.5830A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000366425.4:c.529A= (GP1BB) MANE Select ENSP00000383382.2:p.Arg177=
ENST00000366425.3:c.529A= (GP1BB) ENSP00000383382.2:p.Arg177=
ENST00000431044.5:c.*1614A= (SEPTIN5) ENSP00000399685.1:n.*1614A=
NM_000407.4:c.529A= , LRG_478t1:c.529A= (GP1BB) NP_000398.1:p.Arg177=
NR_037611.1:n.4269A=
NR_037612.1:n.2773A=
NM_000407.5:c.529A= (GP1BB) MANE Select NP_000398.1:p.Arg177=