Canonical Allele Identifier: CA2396008272
Gene: GP1BB HGNC NCBI
SEPTIN5 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.19723712G= , CM000684.2:g.19723712G= GRCh38
NC_000022.10:g.19711235G= , CM000684.1:g.19711235G= GRCh37
NC_000022.9:g.18091235G= NCBI36
NG_007974.1:g.5170G= , LRG_478:g.5170G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000366425.4:c.10+133G= (GP1BB) MANE Select ENSP00000383382.2:n.10+133G=
ENST00000366425.3:c.10+133G= (GP1BB) ENSP00000383382.2:n.10+133G=
ENST00000431044.5:c.*1095+133G= (SEPTIN5) ENSP00000399685.1:n.*1095+133G=
ENST00000455843.5:c.*1095+133G= (SEPTIN5) ENSP00000391731.1:n.*1095+133G=
ENST00000470814.1:n.1982+133G= (SEPTIN5)
NM_000407.4:c.10+133G= , LRG_478t1:c.10+133G= (GP1BB) NP_000398.1:n.10+133G=
NR_037611.1:n.3750+133G=
NR_037612.1:n.2254+133G=
NM_000407.5:c.10+133G= (GP1BB) MANE Select NP_000398.1:n.10+133G=
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