Canonical Allele Identifier: CA2396008631
Gene: GP1BB HGNC NCBI
SEPTIN5 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.19724379G= , CM000684.2:g.19724379G= GRCh38
NC_000022.10:g.19711902G= , CM000684.1:g.19711902G= GRCh37
NC_000022.9:g.18091902G= NCBI36
NG_007974.1:g.5837G= , LRG_478:g.5837G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000366425.4:c.536G= (GP1BB) MANE Select ENSP00000383382.2:p.Arg179=
ENST00000366425.3:c.536G= (GP1BB) ENSP00000383382.2:p.Arg179=
ENST00000431044.5:c.*1621G= (SEPTIN5) ENSP00000399685.1:n.*1621G=
NM_000407.4:c.536G= , LRG_478t1:c.536G= (GP1BB) NP_000398.1:p.Arg179=
NR_037611.1:n.4276G=
NR_037612.1:n.2780G=
NM_000407.5:c.536G= (GP1BB) MANE Select NP_000398.1:p.Arg179=
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