Canonical Allele Identifier: CA2343355853
Gene: BRSK1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55308677C= , CM000681.2:g.55308677C= GRCh38
NC_000019.9:g.55820045C= , CM000681.1:g.55820045C= GRCh37
NC_000019.8:g.60511857C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000309383.6:c.2128C= MANE Select ENSP00000310649.1:p.Gln710=
ENST00000309383.5:c.2128C= ENSP00000310649.1:p.Gln710=
ENST00000326848.7:c.1213C= ENSP00000320853.7:p.Gln405=
ENST00000590333.5:c.2176C= ENSP00000468190.1:p.Gln726=
NM_032430.1:c.2128C= NP_115806.1:p.Gln710=
XM_005259327.2:c.1858C= XP_005259384.1:p.Gln620=
XM_011527395.1:c.1885C= XP_011525697.1:p.Gln629=
XR_430213.2:n.2111C=
XM_005259327.3:c.1858C= XP_005259384.1:p.Gln620=
XM_011527395.2:c.1600C= XP_011525697.2:p.Gln534=
XM_024451739.1:c.1903C= XP_024307507.1:p.Gln635=
XR_430213.4:n.2409C=
NM_032430.2:c.2128C= MANE Select NP_115806.1:p.Gln710=