Canonical Allele Identifier: CA883744759
Gene: BRSK1 HGNC NCBI

Linked Data

dbSNP Id: rs1427515176

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55308806dup , CM000681.2:g.55308806dup GRCh38
NC_000019.9:g.55820174dup , CM000681.1:g.55820174dup GRCh37
NC_000019.8:g.60511986dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000309383.6:c.2179+78dup MANE Select ENSP00000310649.1:n.2179+78dup
ENST00000309383.5:c.2179+78dup ENSP00000310649.1:n.2179+78dup
ENST00000326848.7:c.1264+78dup ENSP00000320853.7:n.1264+78dup
ENST00000590333.5:c.2227+78dup ENSP00000468190.1:n.2227+78dup
NM_032430.1:c.2179+78dup NP_115806.1:n.2179+78dup
XM_005259327.2:c.1909+78dup XP_005259384.1:n.1909+78dup
XM_011527395.1:c.1936+78dup XP_011525697.1:n.1936+78dup
XR_430213.2:n.2162+78dup
XM_005259327.3:c.1909+78dup XP_005259384.1:n.1909+78dup
XM_011527395.2:c.1651+78dup XP_011525697.2:n.1651+78dup
XM_024451739.1:c.1954+78dup XP_024307507.1:n.1954+78dup
XR_430213.4:n.2460+78dup
NM_032430.2:c.2179+78dup MANE Select NP_115806.1:n.2179+78dup