Canonical Allele Identifier: CA2343355855
Gene: BRSK1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55308682A= , CM000681.2:g.55308682A= GRCh38
NC_000019.9:g.55820050A= , CM000681.1:g.55820050A= GRCh37
NC_000019.8:g.60511862A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000309383.6:c.2133A= MANE Select ENSP00000310649.1:p.Ala711=
ENST00000309383.5:c.2133A= ENSP00000310649.1:p.Ala711=
ENST00000326848.7:c.1218A= ENSP00000320853.7:p.Ala406=
ENST00000590333.5:c.2181A= ENSP00000468190.1:p.Ala727=
NM_032430.1:c.2133A= NP_115806.1:p.Ala711=
XM_005259327.2:c.1863A= XP_005259384.1:p.Ala621=
XM_011527395.1:c.1890A= XP_011525697.1:p.Ala630=
XR_430213.2:n.2116A=
XM_005259327.3:c.1863A= XP_005259384.1:p.Ala621=
XM_011527395.2:c.1605A= XP_011525697.2:p.Ala535=
XM_024451739.1:c.1908A= XP_024307507.1:p.Ala636=
XR_430213.4:n.2414A=
NM_032430.2:c.2133A= MANE Select NP_115806.1:p.Ala711=