Canonical Allele Identifier: CA2343355865
Gene: BRSK1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55308712C= , CM000681.2:g.55308712C= GRCh38
NC_000019.9:g.55820080C= , CM000681.1:g.55820080C= GRCh37
NC_000019.8:g.60511892C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000309383.6:c.2163C= MANE Select ENSP00000310649.1:p.Ser721=
ENST00000309383.5:c.2163C= ENSP00000310649.1:p.Ser721=
ENST00000326848.7:c.1248C= ENSP00000320853.7:p.Ser416=
ENST00000590333.5:c.2211C= ENSP00000468190.1:p.Ser737=
NM_032430.1:c.2163C= NP_115806.1:p.Ser721=
XM_005259327.2:c.1893C= XP_005259384.1:p.Ser631=
XM_011527395.1:c.1920C= XP_011525697.1:p.Ser640=
XR_430213.2:n.2146C=
XM_005259327.3:c.1893C= XP_005259384.1:p.Ser631=
XM_011527395.2:c.1635C= XP_011525697.2:p.Ser545=
XM_024451739.1:c.1938C= XP_024307507.1:p.Ser646=
XR_430213.4:n.2444C=
NM_032430.2:c.2163C= MANE Select NP_115806.1:p.Ser721=