Canonical Allele Identifier: CA2396008575
Gene: GP1BB HGNC NCBI
SEPTIN5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.19724278G= , CM000684.2:g.19724278G= GRCh38
NC_000022.10:g.19711801G= , CM000684.1:g.19711801G= GRCh37
NC_000022.9:g.18091801G= NCBI36
NG_007974.1:g.5736G= , LRG_478:g.5736G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000366425.4:c.435G= (GP1BB) MANE Select ENSP00000383382.2:p.Pro145=
ENST00000366425.3:c.435G= (GP1BB) ENSP00000383382.2:p.Pro145=
ENST00000431044.5:c.*1520G= (SEPTIN5) ENSP00000399685.1:n.*1520G=
NM_000407.4:c.435G= , LRG_478t1:c.435G= (GP1BB) NP_000398.1:p.Pro145=
NR_037611.1:n.4175G=
NR_037612.1:n.2679G=
NM_000407.5:c.435G= (GP1BB) MANE Select NP_000398.1:p.Pro145=