Canonical Allele Identifier: CA2317588627

Gene: STK11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1218583_1218596delinsCTTCCCGTCTCCTT , CM000681.2:g.1218583_1218596delinsCTTCCCGTCTCCTT	GRCh38
NC_000019.9:g.1218582_1218595delinsCTTCCCGTCTCCTT , CM000681.1:g.1218582_1218595delinsCTTCCCGTCTCCTT	GRCh37
NC_000019.8:g.1169582_1169595delinsCTTCCCGTCTCCTT	NCBI36
NG_007460.2:g.34177_34190delinsCTTCCCGTCTCCTT , LRG_319:g.34177_34190delinsCTTCCCGTCTCCTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.374+83_374+96delinsCTTCCCGTCTCCTT	ENSP00000490268.2:n.374+83_374+96delinsCTTCCCGTCTCCTT
ENST00000585748.3:c.2+83_2+96delinsCTTCCCGTCTCCTT	ENSP00000477641.2:n.2+83_2+96delinsCTTCCCGTCTCCTT
ENST00000585851.2:c.291-1790_291-1777delinsCTTCCCGTCTCCTT	ENSP00000467912.2:n.291-1790_291-1777delinsCTTCCCGTCTCCTT
ENST00000326873.12:c.374+83_374+96delinsCTTCCCGTCTCCTT MANE Select	ENSP00000324856.6:n.374+83_374+96delinsCTTCCCGTCTCCTT
ENST00000652231.1:c.374+83_374+96delinsCTTCCCGTCTCCTT	ENSP00000498804.1:n.374+83_374+96delinsCTTCCCGTCTCCTT
ENST00000326873.11:c.374+83_374+96delinsCTTCCCGTCTCCTT	ENSP00000324856.6:n.374+83_374+96delinsCTTCCCGTCTCCTT
ENST00000585748.2:c.2+83_2+96delinsCTTCCCGTCTCCTT	ENSP00000477641.1:n.2+83_2+96delinsCTTCCCGTCTCCTT
ENST00000585851.1:c.291-1790_291-1777delinsCTTCCCGTCTCCTT	ENSP00000467912.1:n.291-1790_291-1777delinsCTTCCCGTCTCCTT
ENST00000586243.5:c.374+83_374+96delinsCTTCCCGTCTCCTT	ENSP00000467240.2:n.374+83_374+96delinsCTTCCCGTCTCCTT
ENST00000586358.5:n.197+83_197+96delinsCTTCCCGTCTCCTT
ENST00000589152.5:n.464+83_464+96delinsCTTCCCGTCTCCTT
ENST00000593219.5:c.*199+83_*199+96delinsCTTCCCGTCTCCTT	ENSP00000466610.1:n.*199+83_*199+96delinsCTTCCCGTCTCCTT
NM_000455.4:c.374+83_374+96delinsCTTCCCGTCTCCTT , LRG_319t1:c.374+83_374+96delinsCTTCCCGTCTCCTT	NP_000446.1:n.374+83_374+96delinsCTTCCCGTCTCCTT
XM_005259617.1:c.374+83_374+96delinsCTTCCCGTCTCCTT	XP_005259674.1:n.374+83_374+96delinsCTTCCCGTCTCCTT
XM_005259618.3:c.374+83_374+96delinsCTTCCCGTCTCCTT	XP_005259675.1:n.374+83_374+96delinsCTTCCCGTCTCCTT
XM_011528209.1:c.152+83_152+96delinsCTTCCCGTCTCCTT	XP_011526511.1:n.152+83_152+96delinsCTTCCCGTCTCCTT
XR_936204.1:n.999+83_999+96delinsCTTCCCGTCTCCTT
XM_005259617.3:c.374+83_374+96delinsCTTCCCGTCTCCTT	XP_005259674.1:n.374+83_374+96delinsCTTCCCGTCTCCTT
XM_011528209.2:c.152+83_152+96delinsCTTCCCGTCTCCTT	XP_011526511.1:n.152+83_152+96delinsCTTCCCGTCTCCTT
XR_001753738.2:n.999+83_999+96delinsCTTCCCGTCTCCTT
XR_001753739.1:n.999+83_999+96delinsCTTCCCGTCTCCTT
XR_001753740.2:n.999+83_999+96delinsCTTCCCGTCTCCTT
NM_000455.5:c.374+83_374+96delinsCTTCCCGTCTCCTT MANE Select	NP_000446.1:n.374+83_374+96delinsCTTCCCGTCTCCTT