Canonical Allele Identifier: CA2343355993
Gene: BRSK1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55308809_55308822delinsTGGGTGGCGGGGGG , CM000681.2:g.55308809_55308822delinsTGGGTGGCGGGGGG GRCh38
NC_000019.9:g.55820177_55820190delinsTGGGTGGCGGGGGG , CM000681.1:g.55820177_55820190delinsTGGGTGGCGGGGGG GRCh37
NC_000019.8:g.60511989_60512002delinsTGGGTGGCGGGGGG NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000309383.6:c.2179+81_2179+94delinsTGGGTGGCGGGGGG MANE Select ENSP00000310649.1:n.2179+81_2179+94delinsTGGGTGGCGGGGGG
ENST00000309383.5:c.2179+81_2179+94delinsTGGGTGGCGGGGGG ENSP00000310649.1:n.2179+81_2179+94delinsTGGGTGGCGGGGGG
ENST00000326848.7:c.1264+81_1264+94delinsTGGGTGGCGGGGGG ENSP00000320853.7:n.1264+81_1264+94delinsTGGGTGGCGGGGGG
ENST00000590333.5:c.2227+81_2227+94delinsTGGGTGGCGGGGGG ENSP00000468190.1:n.2227+81_2227+94delinsTGGGTGGCGGGGGG
NM_032430.1:c.2179+81_2179+94delinsTGGGTGGCGGGGGG NP_115806.1:n.2179+81_2179+94delinsTGGGTGGCGGGGGG
XM_005259327.2:c.1909+81_1909+94delinsTGGGTGGCGGGGGG XP_005259384.1:n.1909+81_1909+94delinsTGGGTGGCGGGGGG
XM_011527395.1:c.1936+81_1936+94delinsTGGGTGGCGGGGGG XP_011525697.1:n.1936+81_1936+94delinsTGGGTGGCGGGGGG
XR_430213.2:n.2162+81_2162+94delinsTGGGTGGCGGGGGG
XM_005259327.3:c.1909+81_1909+94delinsTGGGTGGCGGGGGG XP_005259384.1:n.1909+81_1909+94delinsTGGGTGGCGGGGGG
XM_011527395.2:c.1651+81_1651+94delinsTGGGTGGCGGGGGG XP_011525697.2:n.1651+81_1651+94delinsTGGGTGGCGGGGGG
XM_024451739.1:c.1954+81_1954+94delinsTGGGTGGCGGGGGG XP_024307507.1:n.1954+81_1954+94delinsTGGGTGGCGGGGGG
XR_430213.4:n.2460+81_2460+94delinsTGGGTGGCGGGGGG
NM_032430.2:c.2179+81_2179+94delinsTGGGTGGCGGGGGG MANE Select NP_115806.1:n.2179+81_2179+94delinsTGGGTGGCGGGGGG