Canonical Allele Identifier: CA407462246
Gene: BRSK1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.55308769del (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55308773del , CM000681.2:g.55308773del GRCh38
NC_000019.9:g.55820141del , CM000681.1:g.55820141del GRCh37
NC_000019.8:g.60511953del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000309383.6:c.2179+45del MANE Select ENSP00000310649.1:n.2179+45del
ENST00000309383.5:c.2179+45del ENSP00000310649.1:n.2179+45del
ENST00000326848.7:c.1264+45del ENSP00000320853.7:n.1264+45del
ENST00000590333.5:c.2227+45del ENSP00000468190.1:n.2227+45del
NM_032430.1:c.2179+45del NP_115806.1:n.2179+45del
XM_005259327.2:c.1909+45del XP_005259384.1:n.1909+45del
XM_011527395.1:c.1936+45del XP_011525697.1:n.1936+45del
XR_430213.2:n.2162+45del
XM_005259327.3:c.1909+45del XP_005259384.1:n.1909+45del
XM_011527395.2:c.1651+45del XP_011525697.2:n.1651+45del
XM_024451739.1:c.1954+45del XP_024307507.1:n.1954+45del
XR_430213.4:n.2460+45del
NM_032430.2:c.2179+45del MANE Select NP_115806.1:n.2179+45del