Canonical Allele Identifier: CA2343355767
Gene: BRSK1 HGNC NCBI

Linked Data

dbSNP Id: rs1339348275

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55308539del , CM000681.2:g.55308539del GRCh38
NC_000019.9:g.55819907del , CM000681.1:g.55819907del GRCh37
NC_000019.8:g.60511719del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000309383.6:c.2090-100del MANE Select ENSP00000310649.1:n.2090-100del
ENST00000309383.5:c.2090-100del ENSP00000310649.1:n.2090-100del
ENST00000326848.7:c.1175-100del ENSP00000320853.7:n.1175-100del
ENST00000590333.5:c.2138-100del ENSP00000468190.1:n.2138-100del
NM_032430.1:c.2090-100del NP_115806.1:n.2090-100del
XM_005259327.2:c.1820-100del XP_005259384.1:n.1820-100del
XM_011527395.1:c.1847-100del XP_011525697.1:n.1847-100del
XR_430213.2:n.2073-100del
XM_005259327.3:c.1820-100del XP_005259384.1:n.1820-100del
XM_011527395.2:c.1562-100del XP_011525697.2:n.1562-100del
XM_024451739.1:c.1865-100del XP_024307507.1:n.1865-100del
XR_430213.4:n.2371-100del
NM_032430.2:c.2090-100del MANE Select NP_115806.1:n.2090-100del