Canonical Allele Identifier: CA992489807

Gene: STK11

Linked Data

• dbSNP Id: rs2080760661
• gnomAD v3: 19-1218703-CTG-C
• gnomAD v4: 19-1218703-CTG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1218707_1218708del , CM000681.2:g.1218707_1218708del	GRCh38
NC_000019.9:g.1218706_1218707del , CM000681.1:g.1218706_1218707del	GRCh37
NC_000019.8:g.1169706_1169707del	NCBI36
NG_007460.2:g.34301_34302del , LRG_319:g.34301_34302del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.374+207_374+208del	ENSP00000490268.2:n.374+207_374+208del
ENST00000585748.3:c.2+207_2+208del	ENSP00000477641.2:n.2+207_2+208del
ENST00000585851.2:c.291-1666_291-1665del	ENSP00000467912.2:n.291-1666_291-1665del
ENST00000326873.12:c.374+207_374+208del MANE Select	ENSP00000324856.6:n.374+207_374+208del
ENST00000652231.1:c.374+207_374+208del	ENSP00000498804.1:n.374+207_374+208del
ENST00000326873.11:c.374+207_374+208del	ENSP00000324856.6:n.374+207_374+208del
ENST00000585748.2:c.2+207_2+208del	ENSP00000477641.1:n.2+207_2+208del
ENST00000585851.1:c.291-1666_291-1665del	ENSP00000467912.1:n.291-1666_291-1665del
ENST00000586243.5:c.374+207_374+208del	ENSP00000467240.2:n.374+207_374+208del
ENST00000586358.5:n.197+207_197+208del
ENST00000589152.5:n.464+207_464+208del
ENST00000593219.5:c.*199+207_*199+208del	ENSP00000466610.1:n.*199+207_*199+208del
NM_000455.4:c.374+207_374+208del , LRG_319t1:c.374+207_374+208del	NP_000446.1:n.374+207_374+208del
XM_005259617.1:c.374+207_374+208del	XP_005259674.1:n.374+207_374+208del
XM_005259618.3:c.374+207_374+208del	XP_005259675.1:n.374+207_374+208del
XM_011528209.1:c.152+207_152+208del	XP_011526511.1:n.152+207_152+208del
XR_936204.1:n.999+207_999+208del
XM_005259617.3:c.374+207_374+208del	XP_005259674.1:n.374+207_374+208del
XM_011528209.2:c.152+207_152+208del	XP_011526511.1:n.152+207_152+208del
XR_001753738.2:n.999+207_999+208del
XR_001753739.1:n.999+207_999+208del
XR_001753740.2:n.999+207_999+208del
NM_000455.5:c.374+207_374+208del MANE Select	NP_000446.1:n.374+207_374+208del