Canonical Allele Identifier: CA2317591528

Gene: STK11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1223099_1223105delinsCGGCGCG , CM000681.2:g.1223099_1223105delinsCGGCGCG	GRCh38
NC_000019.9:g.1223098_1223104delinsCGGCGCG , CM000681.1:g.1223098_1223104delinsCGGCGCG	GRCh37
NC_000019.8:g.1174098_1174104delinsCGGCGCG	NCBI36
NG_007460.2:g.38693_38699delinsCGGCGCG , LRG_319:g.38693_38699delinsCGGCGCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.1035_1041delinsCGGCGCG	ENSP00000490268.2:p.His345=
ENST00000585748.3:c.663_669delinsCGGCGCG	ENSP00000477641.2:p.His221=
ENST00000585851.2:c.861_867delinsCGGCGCG	ENSP00000467912.2:p.His287=
ENST00000326873.12:c.1035_1041delinsCGGCGCG MANE Select	ENSP00000324856.6:p.His345=
ENST00000652231.1:c.1035_1041delinsCGGCGCG	ENSP00000498804.1:p.His345=
ENST00000326873.11:c.1035_1041delinsCGGCGCG	ENSP00000324856.6:p.His345=
ENST00000586243.5:c.1035_1041delinsCGGCGCG	ENSP00000467240.2:p.His345=
ENST00000589152.5:n.1733_1739delinsCGGCGCG
NM_000455.4:c.1035_1041delinsCGGCGCG , LRG_319t1:c.1035_1041delinsCGGCGCG	NP_000446.1:p.His345=
XM_005259617.1:c.1035_1041delinsCGGCGCG	XP_005259674.1:p.His345=
XM_005259618.3:c.1035_1041delinsCGGCGCG	XP_005259675.1:p.His345=
XM_011528209.1:c.813_819delinsCGGCGCG	XP_011526511.1:p.His271=
XR_936204.1:n.1811_1817delinsCGGCGCG
XM_005259617.3:c.1035_1041delinsCGGCGCG	XP_005259674.1:p.His345=
XM_011528209.2:c.813_819delinsCGGCGCG	XP_011526511.1:p.His271=
XR_001753738.2:n.1841_1847delinsCGGCGCG
XR_001753739.1:n.1841_1847delinsCGGCGCG
XR_001753740.2:n.1811_1817delinsCGGCGCG
NM_000455.5:c.1035_1041delinsCGGCGCG MANE Select	NP_000446.1:p.His345=