Canonical Allele Identifier: CA2573320585

Gene: STK11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1221224_1221227dup , CM000681.2:g.1221224_1221227dup	GRCh38
NC_000019.9:g.1221223_1221226dup , CM000681.1:g.1221223_1221226dup	GRCh37
NC_000019.8:g.1172223_1172226dup	NCBI36
NG_007460.2:g.36818_36821dup , LRG_319:g.36818_36821dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.746_749dup	ENSP00000490268.2:p.Gly251HisfsTer16
ENST00000585748.3:c.374_377dup	ENSP00000477641.2:p.Gly127HisfsTer16
ENST00000585851.2:c.572_575dup	ENSP00000467912.2:p.Gly193HisfsTer16
ENST00000326873.12:c.746_749dup MANE Select	ENSP00000324856.6:p.Gly251HisfsTer16
ENST00000652231.1:c.746_749dup	ENSP00000498804.1:p.Gly251HisfsTer16
ENST00000326873.11:c.746_749dup	ENSP00000324856.6:p.Gly251HisfsTer16
ENST00000586243.5:c.746_749dup	ENSP00000467240.2:p.Gly251HisfsTer16
ENST00000586358.5:n.644_647dup
ENST00000589152.5:n.836_839dup
ENST00000591133.2:n.717_720dup
NM_000455.4:c.746_749dup , LRG_319t1:c.746_749dup	NP_000446.1:p.Gly251HisfsTer16
XM_005259617.1:c.746_749dup	XP_005259674.1:p.Gly251HisfsTer16
XM_005259618.3:c.746_749dup	XP_005259675.1:p.Gly251HisfsTer16
XM_011528209.1:c.524_527dup	XP_011526511.1:p.Gly177HisfsTer16
XR_936204.1:n.1371_1374dup
XM_005259617.3:c.746_749dup	XP_005259674.1:p.Gly251HisfsTer16
XM_011528209.2:c.524_527dup	XP_011526511.1:p.Gly177HisfsTer16
XR_001753738.2:n.1371_1374dup
XR_001753739.1:n.1371_1374dup
XR_001753740.2:n.1371_1374dup
NM_000455.5:c.746_749dup MANE Select	NP_000446.1:p.Gly251HisfsTer16