Canonical Allele Identifier: CA508995463
Gene: BRSK1 HGNC NCBI

Linked Data

dbSNP Id: rs1341687453

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55308658G>A , CM000681.2:g.55308658G>A GRCh38
NC_000019.9:g.55820026G>A , CM000681.1:g.55820026G>A GRCh37
NC_000019.8:g.60511838G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000309383.6:c.2109G>A MANE Select ENSP00000310649.1:p.Lys703=
ENST00000309383.5:c.2109G>A ENSP00000310649.1:p.Lys703=
ENST00000326848.7:c.1194G>A ENSP00000320853.7:p.Lys398=
ENST00000590333.5:c.2157G>A ENSP00000468190.1:p.Lys719=
NM_032430.1:c.2109G>A NP_115806.1:p.Lys703=
XM_005259327.2:c.1839G>A XP_005259384.1:p.Lys613=
XM_011527395.1:c.1866G>A XP_011525697.1:p.Lys622=
XR_430213.2:n.2092G>A
XM_005259327.3:c.1839G>A XP_005259384.1:p.Lys613=
XM_011527395.2:c.1581G>A XP_011525697.2:p.Lys527=
XM_024451739.1:c.1884G>A XP_024307507.1:p.Lys628=
XR_430213.4:n.2390G>A
NM_032430.2:c.2109G>A MANE Select NP_115806.1:p.Lys703=