Canonical Allele Identifier: CA513686990
Gene: GP1BB HGNC NCBI
SEPTIN5 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.19711777G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.19724254G>T , CM000684.2:g.19724254G>T GRCh38
NC_000022.10:g.19711777G>T , CM000684.1:g.19711777G>T GRCh37
NC_000022.9:g.18091777G>T NCBI36
NG_007974.1:g.5712G>T , LRG_478:g.5712G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000366425.4:c.411G>T (GP1BB) MANE Select ENSP00000383382.2:p.Leu137=
ENST00000366425.3:c.411G>T (GP1BB) ENSP00000383382.2:p.Leu137=
ENST00000431044.5:c.*1496G>T (SEPTIN5) ENSP00000399685.1:n.*1496G>T
NM_000407.4:c.411G>T , LRG_478t1:c.411G>T (GP1BB) NP_000398.1:p.Leu137=
NR_037611.1:n.4151G>T
NR_037612.1:n.2655G>T
NM_000407.5:c.411G>T (GP1BB) MANE Select NP_000398.1:p.Leu137=