Canonical Allele Identifier: CA2343355852
Gene: BRSK1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55308673C= , CM000681.2:g.55308673C= GRCh38
NC_000019.9:g.55820041C= , CM000681.1:g.55820041C= GRCh37
NC_000019.8:g.60511853C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000309383.6:c.2124C= MANE Select ENSP00000310649.1:p.Thr708=
ENST00000309383.5:c.2124C= ENSP00000310649.1:p.Thr708=
ENST00000326848.7:c.1209C= ENSP00000320853.7:p.Thr403=
ENST00000590333.5:c.2172C= ENSP00000468190.1:p.Thr724=
NM_032430.1:c.2124C= NP_115806.1:p.Thr708=
XM_005259327.2:c.1854C= XP_005259384.1:p.Thr618=
XM_011527395.1:c.1881C= XP_011525697.1:p.Thr627=
XR_430213.2:n.2107C=
XM_005259327.3:c.1854C= XP_005259384.1:p.Thr618=
XM_011527395.2:c.1596C= XP_011525697.2:p.Thr532=
XM_024451739.1:c.1899C= XP_024307507.1:p.Thr633=
XR_430213.4:n.2405C=
NM_032430.2:c.2124C= MANE Select NP_115806.1:p.Thr708=