Canonical Allele Identifier: CA410676358

Gene: GP1BB SEPTIN5

Linked Data

• gnomAD v4: 22-19723931-T-C
• MyVariant Identifiers: chr22:g.19711454T>C (hg19) ; chr22:g.19723931T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19723931T>C , CM000684.2:g.19723931T>C	GRCh38
NC_000022.10:g.19711454T>C , CM000684.1:g.19711454T>C	GRCh37
NC_000022.9:g.18091454T>C	NCBI36
NG_007974.1:g.5389T>C , LRG_478:g.5389T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366425.4:c.88T>C (GP1BB) MANE Select	ENSP00000383382.2:p.Cys30Arg
ENST00000366425.3:c.88T>C (GP1BB)	ENSP00000383382.2:p.Cys30Arg
ENST00000431044.5:c.*1173T>C (SEPTIN5)	ENSP00000399685.1:n.*1173T>C
ENST00000455843.5:c.*1173T>C (SEPTIN5)	ENSP00000391731.1:n.*1173T>C
ENST00000470814.1:n.2060T>C (SEPTIN5)
NM_000407.4:c.88T>C , LRG_478t1:c.88T>C (GP1BB)	NP_000398.1:p.Cys30Arg
NR_037611.1:n.3828T>C
NR_037612.1:n.2332T>C
NM_000407.5:c.88T>C (GP1BB) MANE Select	NP_000398.1:p.Cys30Arg