Canonical Allele Identifier: CA322079688

Gene: GP1BB SEPTIN5

Linked Data

• dbSNP Id: rs902737789
• gnomAD v3: 22-19723788-G-C
• gnomAD v4: 22-19723788-G-C
• MyVariant Identifiers: chr22:g.19711311G>C (hg19) ; chr22:g.19723788G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19723788G>C , CM000684.2:g.19723788G>C	GRCh38
NC_000022.10:g.19711311G>C , CM000684.1:g.19711311G>C	GRCh37
NC_000022.9:g.18091311G>C	NCBI36
NG_007974.1:g.5246G>C , LRG_478:g.5246G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366425.4:c.11-66G>C (GP1BB) MANE Select	ENSP00000383382.2:n.11-66G>C
ENST00000366425.3:c.11-66G>C (GP1BB)	ENSP00000383382.2:n.11-66G>C
ENST00000431044.5:c.*1096-66G>C (SEPTIN5)	ENSP00000399685.1:n.*1096-66G>C
ENST00000455843.5:c.*1096-66G>C (SEPTIN5)	ENSP00000391731.1:n.*1096-66G>C
ENST00000470814.1:n.1983-66G>C (SEPTIN5)
NM_000407.4:c.11-66G>C , LRG_478t1:c.11-66G>C (GP1BB)	NP_000398.1:n.11-66G>C
NR_037611.1:n.3751-66G>C
NR_037612.1:n.2255-66G>C
NM_000407.5:c.11-66G>C (GP1BB) MANE Select	NP_000398.1:n.11-66G>C