Canonical Allele Identifier: CA2343355851
Gene: BRSK1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55308669A= , CM000681.2:g.55308669A= GRCh38
NC_000019.9:g.55820037A= , CM000681.1:g.55820037A= GRCh37
NC_000019.8:g.60511849A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000309383.6:c.2120A= MANE Select ENSP00000310649.1:p.Glu707=
ENST00000309383.5:c.2120A= ENSP00000310649.1:p.Glu707=
ENST00000326848.7:c.1205A= ENSP00000320853.7:p.Glu402=
ENST00000590333.5:c.2168A= ENSP00000468190.1:p.Glu723=
NM_032430.1:c.2120A= NP_115806.1:p.Glu707=
XM_005259327.2:c.1850A= XP_005259384.1:p.Glu617=
XM_011527395.1:c.1877A= XP_011525697.1:p.Glu626=
XR_430213.2:n.2103A=
XM_005259327.3:c.1850A= XP_005259384.1:p.Glu617=
XM_011527395.2:c.1592A= XP_011525697.2:p.Glu531=
XM_024451739.1:c.1895A= XP_024307507.1:p.Glu632=
XR_430213.4:n.2401A=
NM_032430.2:c.2120A= MANE Select NP_115806.1:p.Glu707=