Canonical Allele Identifier: CA2343355845
Gene: BRSK1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55308657A= , CM000681.2:g.55308657A= GRCh38
NC_000019.9:g.55820025A= , CM000681.1:g.55820025A= GRCh37
NC_000019.8:g.60511837A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000309383.6:c.2108A= MANE Select ENSP00000310649.1:p.Lys703=
ENST00000309383.5:c.2108A= ENSP00000310649.1:p.Lys703=
ENST00000326848.7:c.1193A= ENSP00000320853.7:p.Lys398=
ENST00000590333.5:c.2156A= ENSP00000468190.1:p.Lys719=
NM_032430.1:c.2108A= NP_115806.1:p.Lys703=
XM_005259327.2:c.1838A= XP_005259384.1:p.Lys613=
XM_011527395.1:c.1865A= XP_011525697.1:p.Lys622=
XR_430213.2:n.2091A=
XM_005259327.3:c.1838A= XP_005259384.1:p.Lys613=
XM_011527395.2:c.1580A= XP_011525697.2:p.Lys527=
XM_024451739.1:c.1883A= XP_024307507.1:p.Lys628=
XR_430213.4:n.2389A=
NM_032430.2:c.2108A= MANE Select NP_115806.1:p.Lys703=