Canonical Allele Identifier: CA2317593746

Gene: STK11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1226572_1226584delinsGGCCCCCAACCCT , CM000681.2:g.1226572_1226584delinsGGCCCCCAACCCT	GRCh38
NC_000019.9:g.1226571_1226583delinsGGCCCCCAACCCT , CM000681.1:g.1226571_1226583delinsGGCCCCCAACCCT	GRCh37
NC_000019.8:g.1177571_1177583delinsGGCCCCCAACCCT	NCBI36
NG_007460.2:g.42166_42178delinsGGCCCCCAACCCT , LRG_319:g.42166_42178delinsGGCCCCCAACCCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.*2828_*2840delinsGGCCCCCAACCCT	ENSP00000490268.2:n.*2828_*2840delinsGGCCCCCAACCCT
ENST00000585748.3:c.855_867delinsGGCCCCCAACCCT	ENSP00000477641.2:p.Arg285=
ENST00000585851.2:c.1053_1065delinsGGCCCCCAACCCT	ENSP00000467912.2:p.Arg351=
ENST00000326873.12:c.1227_1239delinsGGCCCCCAACCCT MANE Select	ENSP00000324856.6:p.Arg409=
ENST00000326873.11:c.1227_1239delinsGGCCCCCAACCCT	ENSP00000324856.6:p.Arg409=
ENST00000585465.2:n.2960_2972delinsGGCCCCCAACCCT
ENST00000586243.5:c.1226_1238delinsGGCCCCCAACCCT	ENSP00000467240.2:p.Gly409=
ENST00000589152.5:n.1925_1937delinsGGCCCCCAACCCT
NM_000455.4:c.1227_1239delinsGGCCCCCAACCCT , LRG_319t1:c.1227_1239delinsGGCCCCCAACCCT	NP_000446.1:p.Arg409=
XM_005259617.1:c.1222_1234delinsGGCCCCCAACCCT	XP_005259674.1:p.Gly408=
XM_011528209.1:c.1000_1012delinsGGCCCCCAACCCT	XP_011526511.1:p.Gly334=
XM_005259617.3:c.1222_1234delinsGGCCCCCAACCCT	XP_005259674.1:p.Gly408=
XM_011528209.2:c.1000_1012delinsGGCCCCCAACCCT	XP_011526511.1:p.Gly334=
XR_001753738.2:n.2033_2045delinsGGCCCCCAACCCT
XR_001753740.2:n.2003_2015delinsGGCCCCCAACCCT
NM_000455.5:c.1227_1239delinsGGCCCCCAACCCT MANE Select	NP_000446.1:p.Arg409=