Canonical Allele Identifier: CA2343355553

Gene: BRSK1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55308038_55308039delinsTG , CM000681.2:g.55308038_55308039delinsTG	GRCh38
NC_000019.9:g.55819406_55819407delinsTG , CM000681.1:g.55819406_55819407delinsTG	GRCh37
NC_000019.8:g.60511218_60511219delinsTG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000309383.6:c.2090-601_2090-600delinsTG MANE Select	ENSP00000310649.1:n.2090-601_2090-600delinsTG
ENST00000309383.5:c.2090-601_2090-600delinsTG	ENSP00000310649.1:n.2090-601_2090-600delinsTG
ENST00000326848.7:c.1175-601_1175-600delinsTG	ENSP00000320853.7:n.1175-601_1175-600delinsTG
ENST00000590333.5:c.2138-601_2138-600delinsTG	ENSP00000468190.1:n.2138-601_2138-600delinsTG
NM_032430.1:c.2090-601_2090-600delinsTG	NP_115806.1:n.2090-601_2090-600delinsTG
XM_005259327.2:c.1820-601_1820-600delinsTG	XP_005259384.1:n.1820-601_1820-600delinsTG
XM_011527395.1:c.1847-601_1847-600delinsTG	XP_011525697.1:n.1847-601_1847-600delinsTG
XR_430213.2:n.2073-601_2073-600delinsTG
XM_005259327.3:c.1820-601_1820-600delinsTG	XP_005259384.1:n.1820-601_1820-600delinsTG
XM_011527395.2:c.1562-601_1562-600delinsTG	XP_011525697.2:n.1562-601_1562-600delinsTG
XM_024451739.1:c.1865-601_1865-600delinsTG	XP_024307507.1:n.1865-601_1865-600delinsTG
XR_430213.4:n.2371-601_2371-600delinsTG
NM_032430.2:c.2090-601_2090-600delinsTG MANE Select	NP_115806.1:n.2090-601_2090-600delinsTG