Canonical Allele Identifier: CA2343356049

Gene: BRSK1 TMEM150B

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55308883T= , CM000681.2:g.55308883T=	GRCh38
NC_000019.9:g.55820251T= , CM000681.1:g.55820251T=	GRCh37
NC_000019.8:g.60512063T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000309383.6:c.2179+155T= (BRSK1) MANE Select	ENSP00000310649.1:n.2179+155T=
ENST00000309383.5:c.2179+155T= (BRSK1)	ENSP00000310649.1:n.2179+155T=
ENST00000326848.7:c.1264+155T= (BRSK1)	ENSP00000320853.7:n.1264+155T=
ENST00000590333.5:c.2227+155T= (BRSK1)	ENSP00000468190.1:n.2227+155T=
NM_032430.1:c.2179+155T= (BRSK1)	NP_115806.1:n.2179+155T=
XM_005259327.2:c.1909+155T= (BRSK1)	XP_005259384.1:n.1909+155T=
XM_011527395.1:c.1936+155T= (BRSK1)	XP_011525697.1:n.1936+155T=
XR_430213.2:n.2162+155T= (BRSK1)
XM_005259327.3:c.1909+155T= (BRSK1)	XP_005259384.1:n.1909+155T=
XM_011526850.3:c.*1342A= (TMEM150B)	XP_011525152.1:n.*1342A=
XM_011527395.2:c.1651+155T= (BRSK1)	XP_011525697.2:n.1651+155T=
XM_024451739.1:c.1954+155T= (BRSK1)	XP_024307507.1:n.1954+155T=
XR_430213.4:n.2460+155T= (BRSK1)
NM_032430.2:c.2179+155T= (BRSK1) MANE Select	NP_115806.1:n.2179+155T=