Canonical Allele Identifier: CA915951577

Gene: STK11

Linked Data

• ClinVar Variation Id: 654771
• ClinVar RCV Id: RCV000810792
• dbSNP Id: rs1599924500

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1218402_1218418del , CM000681.2:g.1218402_1218418del	GRCh38
NC_000019.9:g.1218401_1218417del , CM000681.1:g.1218401_1218417del	GRCh37
NC_000019.8:g.1169401_1169417del	NCBI36
NG_007460.2:g.33996_34012del , LRG_319:g.33996_34012del

Transcript Alleles

HGVS	Amino-acid change
ENST00000585465.3:c.291-15_292del
ENST00000585748.3:c.-82-15_-81del
ENST00000585851.2:c.291-1971_291-1955del	ENSP00000467912.2:n.291-1971_291-1955del
ENST00000326873.12:c.291-15_292del
ENST00000652231.1:c.291-15_292del
ENST00000326873.11:c.291-15_292del
ENST00000585748.2:c.-82-15_-81del
ENST00000585851.1:c.291-1971_291-1955del	ENSP00000467912.1:n.291-1971_291-1955del
ENST00000586243.5:c.291-15_292del
ENST00000586358.5:n.114-15_115del
ENST00000589152.5:n.381-15_382del
ENST00000593219.5:c.*116-15_*117del
NM_000455.4:c.291-15_292del , LRG_319t1:c.291-15_292del
XM_005259617.1:c.291-15_292del
XM_005259618.3:c.291-15_292del
XM_011528209.1:c.69-15_70del
XR_936204.1:n.916-15_917del
XM_005259617.3:c.291-15_292del
XM_011528209.2:c.69-15_70del
XR_001753738.2:n.916-15_917del
XR_001753739.1:n.916-15_917del
XR_001753740.2:n.916-15_917del
NM_000455.5:c.291-15_292del