Canonical Allele Identifier: CA513686667
Gene: GP1BB HGNC NCBI
SEPTIN5 HGNC NCBI

Linked Data

gnomAD v4: 22-19723867-G-A
MyVariant Identifiers: chr22:g.19711390G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.19723867G>A , CM000684.2:g.19723867G>A GRCh38
NC_000022.10:g.19711390G>A , CM000684.1:g.19711390G>A GRCh37
NC_000022.9:g.18091390G>A NCBI36
NG_007974.1:g.5325G>A , LRG_478:g.5325G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000366425.4:c.24G>A (GP1BB) MANE Select ENSP00000383382.2:p.Ala8=
ENST00000366425.3:c.24G>A (GP1BB) ENSP00000383382.2:p.Ala8=
ENST00000431044.5:c.*1109G>A (SEPTIN5) ENSP00000399685.1:n.*1109G>A
ENST00000455843.5:c.*1109G>A (SEPTIN5) ENSP00000391731.1:n.*1109G>A
ENST00000470814.1:n.1996G>A (SEPTIN5)
NM_000407.4:c.24G>A , LRG_478t1:c.24G>A (GP1BB) NP_000398.1:p.Ala8=
NR_037611.1:n.3764G>A
NR_037612.1:n.2268G>A
NM_000407.5:c.24G>A (GP1BB) MANE Select NP_000398.1:p.Ala8=
Search 100 bp 5'
Search 100 bp 3'