Canonical Allele Identifier: CA2343355686

Gene: BRSK1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55308343_55308344delinsAT , CM000681.2:g.55308343_55308344delinsAT	GRCh38
NC_000019.9:g.55819711_55819712delinsAT , CM000681.1:g.55819711_55819712delinsAT	GRCh37
NC_000019.8:g.60511523_60511524delinsAT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000309383.6:c.2090-296_2090-295delinsAT MANE Select	ENSP00000310649.1:n.2090-296_2090-295delinsAT
ENST00000309383.5:c.2090-296_2090-295delinsAT	ENSP00000310649.1:n.2090-296_2090-295delinsAT
ENST00000326848.7:c.1175-296_1175-295delinsAT	ENSP00000320853.7:n.1175-296_1175-295delinsAT
ENST00000590333.5:c.2138-296_2138-295delinsAT	ENSP00000468190.1:n.2138-296_2138-295delinsAT
NM_032430.1:c.2090-296_2090-295delinsAT	NP_115806.1:n.2090-296_2090-295delinsAT
XM_005259327.2:c.1820-296_1820-295delinsAT	XP_005259384.1:n.1820-296_1820-295delinsAT
XM_011527395.1:c.1847-296_1847-295delinsAT	XP_011525697.1:n.1847-296_1847-295delinsAT
XR_430213.2:n.2073-296_2073-295delinsAT
XM_005259327.3:c.1820-296_1820-295delinsAT	XP_005259384.1:n.1820-296_1820-295delinsAT
XM_011527395.2:c.1562-296_1562-295delinsAT	XP_011525697.2:n.1562-296_1562-295delinsAT
XM_024451739.1:c.1865-296_1865-295delinsAT	XP_024307507.1:n.1865-296_1865-295delinsAT
XR_430213.4:n.2371-296_2371-295delinsAT
NM_032430.2:c.2090-296_2090-295delinsAT MANE Select	NP_115806.1:n.2090-296_2090-295delinsAT