Canonical Allele Identifier: CA2343355557
Gene: BRSK1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55308041G= , CM000681.2:g.55308041G= GRCh38
NC_000019.9:g.55819409G= , CM000681.1:g.55819409G= GRCh37
NC_000019.8:g.60511221G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000309383.6:c.2090-598G= MANE Select ENSP00000310649.1:n.2090-598G=
ENST00000309383.5:c.2090-598G= ENSP00000310649.1:n.2090-598G=
ENST00000326848.7:c.1175-598G= ENSP00000320853.7:n.1175-598G=
ENST00000590333.5:c.2138-598G= ENSP00000468190.1:n.2138-598G=
NM_032430.1:c.2090-598G= NP_115806.1:n.2090-598G=
XM_005259327.2:c.1820-598G= XP_005259384.1:n.1820-598G=
XM_011527395.1:c.1847-598G= XP_011525697.1:n.1847-598G=
XR_430213.2:n.2073-598G=
XM_005259327.3:c.1820-598G= XP_005259384.1:n.1820-598G=
XM_011527395.2:c.1562-598G= XP_011525697.2:n.1562-598G=
XM_024451739.1:c.1865-598G= XP_024307507.1:n.1865-598G=
XR_430213.4:n.2371-598G=
NM_032430.2:c.2090-598G= MANE Select NP_115806.1:n.2090-598G=