Canonical Allele Identifier: CA997262844

Gene: BRSK1

Linked Data

• gnomAD v3: 19-55308399-T-G
• gnomAD v4: 19-55308399-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55308399T>G , CM000681.2:g.55308399T>G	GRCh38
NC_000019.9:g.55819767T>G , CM000681.1:g.55819767T>G	GRCh37
NC_000019.8:g.60511579T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000309383.6:c.2090-240T>G MANE Select	ENSP00000310649.1:n.2090-240T>G
ENST00000309383.5:c.2090-240T>G	ENSP00000310649.1:n.2090-240T>G
ENST00000326848.7:c.1175-240T>G	ENSP00000320853.7:n.1175-240T>G
ENST00000590333.5:c.2138-240T>G	ENSP00000468190.1:n.2138-240T>G
NM_032430.1:c.2090-240T>G	NP_115806.1:n.2090-240T>G
XM_005259327.2:c.1820-240T>G	XP_005259384.1:n.1820-240T>G
XM_011527395.1:c.1847-240T>G	XP_011525697.1:n.1847-240T>G
XR_430213.2:n.2073-240T>G
XM_005259327.3:c.1820-240T>G	XP_005259384.1:n.1820-240T>G
XM_011527395.2:c.1562-240T>G	XP_011525697.2:n.1562-240T>G
XM_024451739.1:c.1865-240T>G	XP_024307507.1:n.1865-240T>G
XR_430213.4:n.2371-240T>G
NM_032430.2:c.2090-240T>G MANE Select	NP_115806.1:n.2090-240T>G