Canonical Allele Identifier: CA2343356006
Gene: BRSK1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55308822_55308838delinsGCGTGGGTGGCGGGGGC , CM000681.2:g.55308822_55308838delinsGCGTGGGTGGCGGGGGC GRCh38
NC_000019.9:g.55820190_55820206delinsGCGTGGGTGGCGGGGGC , CM000681.1:g.55820190_55820206delinsGCGTGGGTGGCGGGGGC GRCh37
NC_000019.8:g.60512002_60512018delinsGCGTGGGTGGCGGGGGC NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000309383.6:c.2179+94_2179+110delinsGCGTGGGTGGCGGGGGC MANE Select ENSP00000310649.1:n.2179+94_2179+110delinsGCGTGGGTGGCGGGGGC
ENST00000309383.5:c.2179+94_2179+110delinsGCGTGGGTGGCGGGGGC ENSP00000310649.1:n.2179+94_2179+110delinsGCGTGGGTGGCGGGGGC
ENST00000326848.7:c.1264+94_1264+110delinsGCGTGGGTGGCGGGGGC ENSP00000320853.7:n.1264+94_1264+110delinsGCGTGGGTGGCGGGGGC
ENST00000590333.5:c.2227+94_2227+110delinsGCGTGGGTGGCGGGGGC ENSP00000468190.1:n.2227+94_2227+110delinsGCGTGGGTGGCGGGGGC
NM_032430.1:c.2179+94_2179+110delinsGCGTGGGTGGCGGGGGC NP_115806.1:n.2179+94_2179+110delinsGCGTGGGTGGCGGGGGC
XM_005259327.2:c.1909+94_1909+110delinsGCGTGGGTGGCGGGGGC XP_005259384.1:n.1909+94_1909+110delinsGCGTGGGTGGCGGGGGC
XM_011527395.1:c.1936+94_1936+110delinsGCGTGGGTGGCGGGGGC XP_011525697.1:n.1936+94_1936+110delinsGCGTGGGTGGCGGGGGC
XR_430213.2:n.2162+94_2162+110delinsGCGTGGGTGGCGGGGGC
XM_005259327.3:c.1909+94_1909+110delinsGCGTGGGTGGCGGGGGC XP_005259384.1:n.1909+94_1909+110delinsGCGTGGGTGGCGGGGGC
XM_011527395.2:c.1651+94_1651+110delinsGCGTGGGTGGCGGGGGC XP_011525697.2:n.1651+94_1651+110delinsGCGTGGGTGGCGGGGGC
XM_024451739.1:c.1954+94_1954+110delinsGCGTGGGTGGCGGGGGC XP_024307507.1:n.1954+94_1954+110delinsGCGTGGGTGGCGGGGGC
XR_430213.4:n.2460+94_2460+110delinsGCGTGGGTGGCGGGGGC
NM_032430.2:c.2179+94_2179+110delinsGCGTGGGTGGCGGGGGC MANE Select NP_115806.1:n.2179+94_2179+110delinsGCGTGGGTGGCGGGGGC