Canonical Allele Identifier: CA997262937

Gene: BRSK1

Linked Data

• dbSNP Id: rs2088715966
• gnomAD v3: 19-55308820-GGGC-G
• gnomAD v4: 19-55308820-GGGC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55308822_55308824del , CM000681.2:g.55308822_55308824del	GRCh38
NC_000019.9:g.55820190_55820192del , CM000681.1:g.55820190_55820192del	GRCh37
NC_000019.8:g.60512002_60512004del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000309383.6:c.2179+94_2179+96del MANE Select	ENSP00000310649.1:n.2179+94_2179+96del
ENST00000309383.5:c.2179+94_2179+96del	ENSP00000310649.1:n.2179+94_2179+96del
ENST00000326848.7:c.1264+94_1264+96del	ENSP00000320853.7:n.1264+94_1264+96del
ENST00000590333.5:c.2227+94_2227+96del	ENSP00000468190.1:n.2227+94_2227+96del
NM_032430.1:c.2179+94_2179+96del	NP_115806.1:n.2179+94_2179+96del
XM_005259327.2:c.1909+94_1909+96del	XP_005259384.1:n.1909+94_1909+96del
XM_011527395.1:c.1936+94_1936+96del	XP_011525697.1:n.1936+94_1936+96del
XR_430213.2:n.2162+94_2162+96del
XM_005259327.3:c.1909+94_1909+96del	XP_005259384.1:n.1909+94_1909+96del
XM_011527395.2:c.1651+94_1651+96del	XP_011525697.2:n.1651+94_1651+96del
XM_024451739.1:c.1954+94_1954+96del	XP_024307507.1:n.1954+94_1954+96del
XR_430213.4:n.2460+94_2460+96del
NM_032430.2:c.2179+94_2179+96del MANE Select	NP_115806.1:n.2179+94_2179+96del