Canonical Allele Identifier: CA883744290

Gene: BRSK1

Linked Data

• dbSNP Id: rs1246143451
• MyVariant Identifiers: chr19:g.55819712del (hg19) ; chr19:g.55308344del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55308346del , CM000681.2:g.55308346del	GRCh38
NC_000019.9:g.55819714del , CM000681.1:g.55819714del	GRCh37
NC_000019.8:g.60511526del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000309383.6:c.2090-293del MANE Select	ENSP00000310649.1:n.2090-293del
ENST00000309383.5:c.2090-293del	ENSP00000310649.1:n.2090-293del
ENST00000326848.7:c.1175-293del	ENSP00000320853.7:n.1175-293del
ENST00000590333.5:c.2138-293del	ENSP00000468190.1:n.2138-293del
NM_032430.1:c.2090-293del	NP_115806.1:n.2090-293del
XM_005259327.2:c.1820-293del	XP_005259384.1:n.1820-293del
XM_011527395.1:c.1847-293del	XP_011525697.1:n.1847-293del
XR_430213.2:n.2073-293del
XM_005259327.3:c.1820-293del	XP_005259384.1:n.1820-293del
XM_011527395.2:c.1562-293del	XP_011525697.2:n.1562-293del
XM_024451739.1:c.1865-293del	XP_024307507.1:n.1865-293del
XR_430213.4:n.2371-293del
NM_032430.2:c.2090-293del MANE Select	NP_115806.1:n.2090-293del