Canonical Allele Identifier: CA2343355513
Gene: BRSK1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55307987A= , CM000681.2:g.55307987A= GRCh38
NC_000019.9:g.55819355A= , CM000681.1:g.55819355A= GRCh37
NC_000019.8:g.60511167A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000309383.6:c.2090-652A= MANE Select ENSP00000310649.1:n.2090-652A=
ENST00000309383.5:c.2090-652A= ENSP00000310649.1:n.2090-652A=
ENST00000326848.7:c.1175-652A= ENSP00000320853.7:n.1175-652A=
ENST00000590333.5:c.2138-652A= ENSP00000468190.1:n.2138-652A=
NM_032430.1:c.2090-652A= NP_115806.1:n.2090-652A=
XM_005259327.2:c.1820-652A= XP_005259384.1:n.1820-652A=
XM_011527395.1:c.1847-652A= XP_011525697.1:n.1847-652A=
XR_430213.2:n.2073-652A=
XM_005259327.3:c.1820-652A= XP_005259384.1:n.1820-652A=
XM_011527395.2:c.1562-652A= XP_011525697.2:n.1562-652A=
XM_024451739.1:c.1865-652A= XP_024307507.1:n.1865-652A=
XR_430213.4:n.2371-652A=
NM_032430.2:c.2090-652A= MANE Select NP_115806.1:n.2090-652A=