Canonical Allele Identifier: CA513687036

Gene: GP1BB SEPTIN5

Linked Data

• dbSNP Id: rs918532079
• gnomAD v4: 22-19724311-G-A
• MyVariant Identifiers: chr22:g.19711834G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19724311G>A , CM000684.2:g.19724311G>A	GRCh38
NC_000022.10:g.19711834G>A , CM000684.1:g.19711834G>A	GRCh37
NC_000022.9:g.18091834G>A	NCBI36
NG_007974.1:g.5769G>A , LRG_478:g.5769G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366425.4:c.468G>A (GP1BB) MANE Select	ENSP00000383382.2:p.Ala156=
ENST00000366425.3:c.468G>A (GP1BB)	ENSP00000383382.2:p.Ala156=
ENST00000431044.5:c.*1553G>A (SEPTIN5)	ENSP00000399685.1:n.*1553G>A
NM_000407.4:c.468G>A , LRG_478t1:c.468G>A (GP1BB)	NP_000398.1:p.Ala156=
NR_037611.1:n.4208G>A
NR_037612.1:n.2712G>A
NM_000407.5:c.468G>A (GP1BB) MANE Select	NP_000398.1:p.Ala156=