Canonical Allele Identifier: CA2587278247

Gene: BRSK1

Linked Data

• gnomAD v4: 19-55308792-GTGGGTGGCGGGGGGC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55308793_55308807del , CM000681.2:g.55308793_55308807del	GRCh38
NC_000019.9:g.55820161_55820175del , CM000681.1:g.55820161_55820175del	GRCh37
NC_000019.8:g.60511973_60511987del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000309383.6:c.2179+65_2179+79del MANE Select	ENSP00000310649.1:n.2179+65_2179+79del
ENST00000309383.5:c.2179+65_2179+79del	ENSP00000310649.1:n.2179+65_2179+79del
ENST00000326848.7:c.1264+65_1264+79del	ENSP00000320853.7:n.1264+65_1264+79del
ENST00000590333.5:c.2227+65_2227+79del	ENSP00000468190.1:n.2227+65_2227+79del
NM_032430.1:c.2179+65_2179+79del	NP_115806.1:n.2179+65_2179+79del
XM_005259327.2:c.1909+65_1909+79del	XP_005259384.1:n.1909+65_1909+79del
XM_011527395.1:c.1936+65_1936+79del	XP_011525697.1:n.1936+65_1936+79del
XR_430213.2:n.2162+65_2162+79del
XM_005259327.3:c.1909+65_1909+79del	XP_005259384.1:n.1909+65_1909+79del
XM_011527395.2:c.1651+65_1651+79del	XP_011525697.2:n.1651+65_1651+79del
XM_024451739.1:c.1954+65_1954+79del	XP_024307507.1:n.1954+65_1954+79del
XR_430213.4:n.2460+65_2460+79del
NM_032430.2:c.2179+65_2179+79del MANE Select	NP_115806.1:n.2179+65_2179+79del