Canonical Allele Identifier: CA407462125

Gene: BRSK1

Linked Data

• dbSNP Id: rs2088706481
• gnomAD v3: 19-55308713-G-A
• gnomAD v4: 19-55308713-G-A
• MyVariant Identifiers: chr19:g.55820081G>A (hg19) ; chr19:g.55308713G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55308713G>A , CM000681.2:g.55308713G>A	GRCh38
NC_000019.9:g.55820081G>A , CM000681.1:g.55820081G>A	GRCh37
NC_000019.8:g.60511893G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000309383.6:c.2164G>A MANE Select	ENSP00000310649.1:p.Val722Met
ENST00000309383.5:c.2164G>A	ENSP00000310649.1:p.Val722Met
ENST00000326848.7:c.1249G>A	ENSP00000320853.7:p.Val417Met
ENST00000590333.5:c.2212G>A	ENSP00000468190.1:p.Val738Met
NM_032430.1:c.2164G>A	NP_115806.1:p.Val722Met
XM_005259327.2:c.1894G>A	XP_005259384.1:p.Val632Met
XM_011527395.1:c.1921G>A	XP_011525697.1:p.Val641Met
XR_430213.2:n.2147G>A
XM_005259327.3:c.1894G>A	XP_005259384.1:p.Val632Met
XM_011527395.2:c.1636G>A	XP_011525697.2:p.Val546Met
XM_024451739.1:c.1939G>A	XP_024307507.1:p.Val647Met
XR_430213.4:n.2445G>A
NM_032430.2:c.2164G>A MANE Select	NP_115806.1:p.Val722Met