Canonical Allele Identifier: CA407461828
Gene: BRSK1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55308656A>T , CM000681.2:g.55308656A>T GRCh38
NC_000019.9:g.55820024A>T , CM000681.1:g.55820024A>T GRCh37
NC_000019.8:g.60511836A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000309383.6:c.2107A>T MANE Select ENSP00000310649.1:p.Lys703Ter
ENST00000309383.5:c.2107A>T ENSP00000310649.1:p.Lys703Ter
ENST00000326848.7:c.1192A>T ENSP00000320853.7:p.Lys398Ter
ENST00000590333.5:c.2155A>T ENSP00000468190.1:p.Lys719Ter
NM_032430.1:c.2107A>T NP_115806.1:p.Lys703Ter
XM_005259327.2:c.1837A>T XP_005259384.1:p.Lys613Ter
XM_011527395.1:c.1864A>T XP_011525697.1:p.Lys622Ter
XR_430213.2:n.2090A>T
XM_005259327.3:c.1837A>T XP_005259384.1:p.Lys613Ter
XM_011527395.2:c.1579A>T XP_011525697.2:p.Lys527Ter
XM_024451739.1:c.1882A>T XP_024307507.1:p.Lys628Ter
XR_430213.4:n.2388A>T
NM_032430.2:c.2107A>T MANE Select NP_115806.1:p.Lys703Ter