Canonical Allele Identifier: CA997262921
Gene: BRSK1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55308805_55308806insCCGTGGGTGGTGGGGG , CM000681.2:g.55308805_55308806insCCGTGGGTGGTGGGGG GRCh38
NC_000019.9:g.55820173_55820174insCCGTGGGTGGTGGGGG , CM000681.1:g.55820173_55820174insCCGTGGGTGGTGGGGG GRCh37
NC_000019.8:g.60511985_60511986insCCGTGGGTGGTGGGGG NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000309383.6:c.2179+77_2179+78insCCGTGGGTGGTGGGGG MANE Select ENSP00000310649.1:n.2179+77_2179+78insCCGTGGGTGGTGGGGG
ENST00000309383.5:c.2179+77_2179+78insCCGTGGGTGGTGGGGG ENSP00000310649.1:n.2179+77_2179+78insCCGTGGGTGGTGGGGG
ENST00000326848.7:c.1264+77_1264+78insCCGTGGGTGGTGGGGG ENSP00000320853.7:n.1264+77_1264+78insCCGTGGGTGGTGGGGG
ENST00000590333.5:c.2227+77_2227+78insCCGTGGGTGGTGGGGG ENSP00000468190.1:n.2227+77_2227+78insCCGTGGGTGGTGGGGG
NM_032430.1:c.2179+77_2179+78insCCGTGGGTGGTGGGGG NP_115806.1:n.2179+77_2179+78insCCGTGGGTGGTGGGGG
XM_005259327.2:c.1909+77_1909+78insCCGTGGGTGGTGGGGG XP_005259384.1:n.1909+77_1909+78insCCGTGGGTGGTGGGGG
XM_011527395.1:c.1936+77_1936+78insCCGTGGGTGGTGGGGG XP_011525697.1:n.1936+77_1936+78insCCGTGGGTGGTGGGGG
XR_430213.2:n.2162+77_2162+78insCCGTGGGTGGTGGGGG
XM_005259327.3:c.1909+77_1909+78insCCGTGGGTGGTGGGGG XP_005259384.1:n.1909+77_1909+78insCCGTGGGTGGTGGGGG
XM_011527395.2:c.1651+77_1651+78insCCGTGGGTGGTGGGGG XP_011525697.2:n.1651+77_1651+78insCCGTGGGTGGTGGGGG
XM_024451739.1:c.1954+77_1954+78insCCGTGGGTGGTGGGGG XP_024307507.1:n.1954+77_1954+78insCCGTGGGTGGTGGGGG
XR_430213.4:n.2460+77_2460+78insCCGTGGGTGGTGGGGG
NM_032430.2:c.2179+77_2179+78insCCGTGGGTGGTGGGGG MANE Select NP_115806.1:n.2179+77_2179+78insCCGTGGGTGGTGGGGG