Canonical Allele Identifier: CA2396008697
Gene: GP1BB HGNC NCBI
SEPTIN5 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.19724469A= , CM000684.2:g.19724469A= GRCh38
NC_000022.10:g.19711992A= , CM000684.1:g.19711992A= GRCh37
NC_000022.9:g.18091992A= NCBI36
NG_007974.1:g.5927A= , LRG_478:g.5927A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000366425.4:c.*5A= (GP1BB) MANE Select ENSP00000383382.2:n.*5A=
ENST00000366425.3:c.*5A= (GP1BB) ENSP00000383382.2:n.*5A=
ENST00000431044.5:c.*1711A= (SEPTIN5) ENSP00000399685.1:n.*1711A=
NM_000407.4:c.*5A= , LRG_478t1:c.*5A= (GP1BB) NP_000398.1:n.*5A=
NR_037611.1:n.4366A=
NR_037612.1:n.2870A=
NM_000407.5:c.*5A= (GP1BB) MANE Select NP_000398.1:n.*5A=
Search 100 bp 5'
Search 100 bp 3'