Canonical Allele Identifier: CA2317589255

Gene: STK11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1219554_1219555delinsGT , CM000681.2:g.1219554_1219555delinsGT	GRCh38
NC_000019.9:g.1219553_1219554delinsGT , CM000681.1:g.1219553_1219554delinsGT	GRCh37
NC_000019.8:g.1170553_1170554delinsGT	NCBI36
NG_007460.2:g.35148_35149delinsGT , LRG_319:g.35148_35149delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.464+141_464+142delinsGT	ENSP00000490268.2:n.464+141_464+142delinsGT
ENST00000585748.3:c.92+141_92+142delinsGT	ENSP00000477641.2:n.92+141_92+142delinsGT
ENST00000585851.2:c.291-819_291-818delinsGT	ENSP00000467912.2:n.291-819_291-818delinsGT
ENST00000326873.12:c.464+141_464+142delinsGT MANE Select	ENSP00000324856.6:n.464+141_464+142delinsGT
ENST00000652231.1:c.464+141_464+142delinsGT	ENSP00000498804.1:n.464+141_464+142delinsGT
ENST00000326873.11:c.464+141_464+142delinsGT	ENSP00000324856.6:n.464+141_464+142delinsGT
ENST00000585851.1:c.291-819_291-818delinsGT	ENSP00000467912.1:n.291-819_291-818delinsGT
ENST00000586243.5:c.464+141_464+142delinsGT	ENSP00000467240.2:n.464+141_464+142delinsGT
ENST00000586358.5:n.287+141_287+142delinsGT
ENST00000589152.5:n.554+141_554+142delinsGT
NM_000455.4:c.464+141_464+142delinsGT , LRG_319t1:c.464+141_464+142delinsGT	NP_000446.1:n.464+141_464+142delinsGT
XM_005259617.1:c.464+141_464+142delinsGT	XP_005259674.1:n.464+141_464+142delinsGT
XM_005259618.3:c.464+141_464+142delinsGT	XP_005259675.1:n.464+141_464+142delinsGT
XM_011528209.1:c.242+141_242+142delinsGT	XP_011526511.1:n.242+141_242+142delinsGT
XR_936204.1:n.1089+141_1089+142delinsGT
XM_005259617.3:c.464+141_464+142delinsGT	XP_005259674.1:n.464+141_464+142delinsGT
XM_011528209.2:c.242+141_242+142delinsGT	XP_011526511.1:n.242+141_242+142delinsGT
XR_001753738.2:n.1089+141_1089+142delinsGT
XR_001753739.1:n.1089+141_1089+142delinsGT
XR_001753740.2:n.1089+141_1089+142delinsGT
NM_000455.5:c.464+141_464+142delinsGT MANE Select	NP_000446.1:n.464+141_464+142delinsGT