Canonical Allele Identifier: CA2343356019
Gene: BRSK1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55308832C= , CM000681.2:g.55308832C= GRCh38
NC_000019.9:g.55820200C= , CM000681.1:g.55820200C= GRCh37
NC_000019.8:g.60512012C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000309383.6:c.2179+104C= MANE Select ENSP00000310649.1:n.2179+104C=
ENST00000309383.5:c.2179+104C= ENSP00000310649.1:n.2179+104C=
ENST00000326848.7:c.1264+104C= ENSP00000320853.7:n.1264+104C=
ENST00000590333.5:c.2227+104C= ENSP00000468190.1:n.2227+104C=
NM_032430.1:c.2179+104C= NP_115806.1:n.2179+104C=
XM_005259327.2:c.1909+104C= XP_005259384.1:n.1909+104C=
XM_011527395.1:c.1936+104C= XP_011525697.1:n.1936+104C=
XR_430213.2:n.2162+104C=
XM_005259327.3:c.1909+104C= XP_005259384.1:n.1909+104C=
XM_011527395.2:c.1651+104C= XP_011525697.2:n.1651+104C=
XM_024451739.1:c.1954+104C= XP_024307507.1:n.1954+104C=
XR_430213.4:n.2460+104C=
NM_032430.2:c.2179+104C= MANE Select NP_115806.1:n.2179+104C=