Canonical Allele Identifier: CA992491106

Gene: STK11

Linked Data

• dbSNP Id: rs2080781982
• gnomAD v3: 19-1221263-AGTT-A
• gnomAD v4: 19-1221263-AGTT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1221267_1221269del , CM000681.2:g.1221267_1221269del	GRCh38
NC_000019.9:g.1221266_1221268del , CM000681.1:g.1221266_1221268del	GRCh37
NC_000019.8:g.1172266_1172268del	NCBI36
NG_007460.2:g.36861_36863del , LRG_319:g.36861_36863del

Transcript Alleles

HGVS	Amino-acid change
ENST00000585465.3:c.789_791del	ENSP00000490268.2:p.Leu263del
ENST00000585748.3:c.417_419del	ENSP00000477641.2:p.Leu139del
ENST00000585851.2:c.615_617del	ENSP00000467912.2:p.Leu205del
ENST00000326873.12:c.789_791del MANE Select	ENSP00000324856.6:p.Leu263del
ENST00000652231.1:c.789_791del	ENSP00000498804.1:p.Leu263del
ENST00000326873.11:c.789_791del	ENSP00000324856.6:p.Leu263del
ENST00000586243.5:c.789_791del	ENSP00000467240.2:p.Leu263del
ENST00000586358.5:n.687_689del
ENST00000589152.5:n.879_881del
ENST00000591133.2:n.760_762del
NM_000455.4:c.789_791del , LRG_319t1:c.789_791del	NP_000446.1:p.Leu263del
XM_005259617.1:c.789_791del	XP_005259674.1:p.Leu263del
XM_005259618.3:c.789_791del	XP_005259675.1:p.Leu263del
XM_011528209.1:c.567_569del	XP_011526511.1:p.Leu189del
XR_936204.1:n.1414_1416del
XM_005259617.3:c.789_791del	XP_005259674.1:p.Leu263del
XM_011528209.2:c.567_569del	XP_011526511.1:p.Leu189del
XR_001753738.2:n.1414_1416del
XR_001753739.1:n.1414_1416del
XR_001753740.2:n.1414_1416del
NM_000455.5:c.789_791del MANE Select	NP_000446.1:p.Leu263del