Canonical Allele Identifier: CA2587278025
Gene: BRSK1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55308584del , CM000681.2:g.55308584del GRCh38
NC_000019.9:g.55819952del , CM000681.1:g.55819952del GRCh37
NC_000019.8:g.60511764del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000309383.6:c.2090-55del MANE Select ENSP00000310649.1:n.2090-55del
ENST00000309383.5:c.2090-55del ENSP00000310649.1:n.2090-55del
ENST00000326848.7:c.1175-55del ENSP00000320853.7:n.1175-55del
ENST00000590333.5:c.2138-55del ENSP00000468190.1:n.2138-55del
NM_032430.1:c.2090-55del NP_115806.1:n.2090-55del
XM_005259327.2:c.1820-55del XP_005259384.1:n.1820-55del
XM_011527395.1:c.1847-55del XP_011525697.1:n.1847-55del
XR_430213.2:n.2073-55del
XM_005259327.3:c.1820-55del XP_005259384.1:n.1820-55del
XM_011527395.2:c.1562-55del XP_011525697.2:n.1562-55del
XM_024451739.1:c.1865-55del XP_024307507.1:n.1865-55del
XR_430213.4:n.2371-55del
NM_032430.2:c.2090-55del MANE Select NP_115806.1:n.2090-55del