Canonical Allele Identifier: CA2396008593
Gene: GP1BB HGNC NCBI
SEPTIN5 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.19724304A= , CM000684.2:g.19724304A= GRCh38
NC_000022.10:g.19711827A= , CM000684.1:g.19711827A= GRCh37
NC_000022.9:g.18091827A= NCBI36
NG_007974.1:g.5762A= , LRG_478:g.5762A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000366425.4:c.461A= (GP1BB) MANE Select ENSP00000383382.2:p.Gln154=
ENST00000366425.3:c.461A= (GP1BB) ENSP00000383382.2:p.Gln154=
ENST00000431044.5:c.*1546A= (SEPTIN5) ENSP00000399685.1:n.*1546A=
NM_000407.4:c.461A= , LRG_478t1:c.461A= (GP1BB) NP_000398.1:p.Gln154=
NR_037611.1:n.4201A=
NR_037612.1:n.2705A=
NM_000407.5:c.461A= (GP1BB) MANE Select NP_000398.1:p.Gln154=
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