Canonical Allele Identifier: CA2317588588

Gene: STK11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1218521_1218532delinsACCGCGGGGCCT , CM000681.2:g.1218521_1218532delinsACCGCGGGGCCT	GRCh38
NC_000019.9:g.1218520_1218531delinsACCGCGGGGCCT , CM000681.1:g.1218520_1218531delinsACCGCGGGGCCT	GRCh37
NC_000019.8:g.1169520_1169531delinsACCGCGGGGCCT	NCBI36
NG_007460.2:g.34115_34126delinsACCGCGGGGCCT , LRG_319:g.34115_34126delinsACCGCGGGGCCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.374+21_374+32delinsACCGCGGGGCCT	ENSP00000490268.2:n.374+21_374+32delinsACCGCGGGGCCT
ENST00000585748.3:c.2+21_2+32delinsACCGCGGGGCCT	ENSP00000477641.2:n.2+21_2+32delinsACCGCGGGGCCT
ENST00000585851.2:c.291-1852_291-1841delinsACCGCGGGGCCT	ENSP00000467912.2:n.291-1852_291-1841delinsACCGCGGGGCCT
ENST00000326873.12:c.374+21_374+32delinsACCGCGGGGCCT MANE Select	ENSP00000324856.6:n.374+21_374+32delinsACCGCGGGGCCT
ENST00000652231.1:c.374+21_374+32delinsACCGCGGGGCCT	ENSP00000498804.1:n.374+21_374+32delinsACCGCGGGGCCT
ENST00000326873.11:c.374+21_374+32delinsACCGCGGGGCCT	ENSP00000324856.6:n.374+21_374+32delinsACCGCGGGGCCT
ENST00000585748.2:c.2+21_2+32delinsACCGCGGGGCCT	ENSP00000477641.1:n.2+21_2+32delinsACCGCGGGGCCT
ENST00000585851.1:c.291-1852_291-1841delinsACCGCGGGGCCT	ENSP00000467912.1:n.291-1852_291-1841delinsACCGCGGGGCCT
ENST00000586243.5:c.374+21_374+32delinsACCGCGGGGCCT	ENSP00000467240.2:n.374+21_374+32delinsACCGCGGGGCCT
ENST00000586358.5:n.197+21_197+32delinsACCGCGGGGCCT
ENST00000589152.5:n.464+21_464+32delinsACCGCGGGGCCT
ENST00000593219.5:c.*199+21_*199+32delinsACCGCGGGGCCT	ENSP00000466610.1:n.*199+21_*199+32delinsACCGCGGGGCCT
NM_000455.4:c.374+21_374+32delinsACCGCGGGGCCT , LRG_319t1:c.374+21_374+32delinsACCGCGGGGCCT	NP_000446.1:n.374+21_374+32delinsACCGCGGGGCCT
XM_005259617.1:c.374+21_374+32delinsACCGCGGGGCCT	XP_005259674.1:n.374+21_374+32delinsACCGCGGGGCCT
XM_005259618.3:c.374+21_374+32delinsACCGCGGGGCCT	XP_005259675.1:n.374+21_374+32delinsACCGCGGGGCCT
XM_011528209.1:c.152+21_152+32delinsACCGCGGGGCCT	XP_011526511.1:n.152+21_152+32delinsACCGCGGGGCCT
XR_936204.1:n.999+21_999+32delinsACCGCGGGGCCT
XM_005259617.3:c.374+21_374+32delinsACCGCGGGGCCT	XP_005259674.1:n.374+21_374+32delinsACCGCGGGGCCT
XM_011528209.2:c.152+21_152+32delinsACCGCGGGGCCT	XP_011526511.1:n.152+21_152+32delinsACCGCGGGGCCT
XR_001753738.2:n.999+21_999+32delinsACCGCGGGGCCT
XR_001753739.1:n.999+21_999+32delinsACCGCGGGGCCT
XR_001753740.2:n.999+21_999+32delinsACCGCGGGGCCT
NM_000455.5:c.374+21_374+32delinsACCGCGGGGCCT MANE Select	NP_000446.1:n.374+21_374+32delinsACCGCGGGGCCT