Canonical Allele Identifier: CA2343355699
Gene: BRSK1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55308371A= , CM000681.2:g.55308371A= GRCh38
NC_000019.9:g.55819739A= , CM000681.1:g.55819739A= GRCh37
NC_000019.8:g.60511551A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000309383.6:c.2090-268A= MANE Select ENSP00000310649.1:n.2090-268A=
ENST00000309383.5:c.2090-268A= ENSP00000310649.1:n.2090-268A=
ENST00000326848.7:c.1175-268A= ENSP00000320853.7:n.1175-268A=
ENST00000590333.5:c.2138-268A= ENSP00000468190.1:n.2138-268A=
NM_032430.1:c.2090-268A= NP_115806.1:n.2090-268A=
XM_005259327.2:c.1820-268A= XP_005259384.1:n.1820-268A=
XM_011527395.1:c.1847-268A= XP_011525697.1:n.1847-268A=
XR_430213.2:n.2073-268A=
XM_005259327.3:c.1820-268A= XP_005259384.1:n.1820-268A=
XM_011527395.2:c.1562-268A= XP_011525697.2:n.1562-268A=
XM_024451739.1:c.1865-268A= XP_024307507.1:n.1865-268A=
XR_430213.4:n.2371-268A=
NM_032430.2:c.2090-268A= MANE Select NP_115806.1:n.2090-268A=