Canonical Allele Identifier: CA2343355783

Gene: BRSK1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55308550T= , CM000681.2:g.55308550T=	GRCh38
NC_000019.9:g.55819918T= , CM000681.1:g.55819918T=	GRCh37
NC_000019.8:g.60511730T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000309383.6:c.2090-89T= MANE Select	ENSP00000310649.1:n.2090-89T=
ENST00000309383.5:c.2090-89T=	ENSP00000310649.1:n.2090-89T=
ENST00000326848.7:c.1175-89T=	ENSP00000320853.7:n.1175-89T=
ENST00000590333.5:c.2138-89T=	ENSP00000468190.1:n.2138-89T=
NM_032430.1:c.2090-89T=	NP_115806.1:n.2090-89T=
XM_005259327.2:c.1820-89T=	XP_005259384.1:n.1820-89T=
XM_011527395.1:c.1847-89T=	XP_011525697.1:n.1847-89T=
XR_430213.2:n.2073-89T=
XM_005259327.3:c.1820-89T=	XP_005259384.1:n.1820-89T=
XM_011527395.2:c.1562-89T=	XP_011525697.2:n.1562-89T=
XM_024451739.1:c.1865-89T=	XP_024307507.1:n.1865-89T=
XR_430213.4:n.2371-89T=
NM_032430.2:c.2090-89T= MANE Select	NP_115806.1:n.2090-89T=