Canonical Allele Identifier: CA2528328748

Gene: BRSK1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55308808_55308822del , CM000681.2:g.55308808_55308822del	GRCh38
NC_000019.9:g.55820176_55820190del , CM000681.1:g.55820176_55820190del	GRCh37
NC_000019.8:g.60511988_60512002del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000309383.6:c.2179+80_2179+94del MANE Select	ENSP00000310649.1:n.2179+80_2179+94del
ENST00000309383.5:c.2179+80_2179+94del	ENSP00000310649.1:n.2179+80_2179+94del
ENST00000326848.7:c.1264+80_1264+94del	ENSP00000320853.7:n.1264+80_1264+94del
ENST00000590333.5:c.2227+80_2227+94del	ENSP00000468190.1:n.2227+80_2227+94del
NM_032430.1:c.2179+80_2179+94del	NP_115806.1:n.2179+80_2179+94del
XM_005259327.2:c.1909+80_1909+94del	XP_005259384.1:n.1909+80_1909+94del
XM_011527395.1:c.1936+80_1936+94del	XP_011525697.1:n.1936+80_1936+94del
XR_430213.2:n.2162+80_2162+94del
XM_005259327.3:c.1909+80_1909+94del	XP_005259384.1:n.1909+80_1909+94del
XM_011527395.2:c.1651+80_1651+94del	XP_011525697.2:n.1651+80_1651+94del
XM_024451739.1:c.1954+80_1954+94del	XP_024307507.1:n.1954+80_1954+94del
XR_430213.4:n.2460+80_2460+94del
NM_032430.2:c.2179+80_2179+94del MANE Select	NP_115806.1:n.2179+80_2179+94del