Canonical Allele Identifier: CA2587278019
Gene: BRSK1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55308580del , CM000681.2:g.55308580del GRCh38
NC_000019.9:g.55819948del , CM000681.1:g.55819948del GRCh37
NC_000019.8:g.60511760del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000309383.6:c.2090-59del MANE Select ENSP00000310649.1:n.2090-59del
ENST00000309383.5:c.2090-59del ENSP00000310649.1:n.2090-59del
ENST00000326848.7:c.1175-59del ENSP00000320853.7:n.1175-59del
ENST00000590333.5:c.2138-59del ENSP00000468190.1:n.2138-59del
NM_032430.1:c.2090-59del NP_115806.1:n.2090-59del
XM_005259327.2:c.1820-59del XP_005259384.1:n.1820-59del
XM_011527395.1:c.1847-59del XP_011525697.1:n.1847-59del
XR_430213.2:n.2073-59del
XM_005259327.3:c.1820-59del XP_005259384.1:n.1820-59del
XM_011527395.2:c.1562-59del XP_011525697.2:n.1562-59del
XM_024451739.1:c.1865-59del XP_024307507.1:n.1865-59del
XR_430213.4:n.2371-59del
NM_032430.2:c.2090-59del MANE Select NP_115806.1:n.2090-59del