Canonical Allele Identifier: CA2697555606

Gene: STK11

Linked Data

• ClinVar Variation Id: 2574115
• ClinVar RCV Id: RCV003485928

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1223100_1223101del , CM000681.2:g.1223100_1223101del	GRCh38
NC_000019.9:g.1223099_1223100del , CM000681.1:g.1223099_1223100del	GRCh37
NC_000019.8:g.1174099_1174100del	NCBI36
NG_007460.2:g.38694_38695del , LRG_319:g.38694_38695del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.1036_1037del	ENSP00000490268.2:p.Gly346ArgfsTer13
ENST00000585748.3:c.664_665del	ENSP00000477641.2:p.Gly222ArgfsTer13
ENST00000585851.2:c.862_863del	ENSP00000467912.2:p.Gly288ArgfsTer13
ENST00000326873.12:c.1036_1037del MANE Select	ENSP00000324856.6:p.Gly346ArgfsTer13
ENST00000652231.1:c.1036_1037del	ENSP00000498804.1:p.Gly346ArgfsTer13
ENST00000326873.11:c.1036_1037del	ENSP00000324856.6:p.Gly346ArgfsTer13
ENST00000586243.5:c.1036_1037del	ENSP00000467240.2:p.Gly346ArgfsTer13
ENST00000589152.5:n.1734_1735del
ENST00000591133.2:n.1007_1008del
NM_000455.4:c.1036_1037del , LRG_319t1:c.1036_1037del	NP_000446.1:p.Gly346ArgfsTer13
XM_005259617.1:c.1036_1037del	XP_005259674.1:p.Gly346ArgfsTer13
XM_005259618.3:c.1036_1037del	XP_005259675.1:p.Gly346ArgfsTer13
XM_011528209.1:c.814_815del	XP_011526511.1:p.Gly272ArgfsTer13
XR_936204.1:n.1812_1813del
XM_005259617.3:c.1036_1037del	XP_005259674.1:p.Gly346ArgfsTer13
XM_011528209.2:c.814_815del	XP_011526511.1:p.Gly272ArgfsTer13
XR_001753738.2:n.1842_1843del
XR_001753739.1:n.1842_1843del
XR_001753740.2:n.1812_1813del
NM_000455.5:c.1036_1037del MANE Select	NP_000446.1:p.Gly346ArgfsTer13