Canonical Allele Identifier: CA2317593522

Gene: STK11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1226268_1226269delinsCG , CM000681.2:g.1226268_1226269delinsCG	GRCh38
NC_000019.9:g.1226267_1226268delinsCG , CM000681.1:g.1226267_1226268delinsCG	GRCh37
NC_000019.8:g.1177267_1177268delinsCG	NCBI36
NG_007460.2:g.41862_41863delinsCG , LRG_319:g.41862_41863delinsCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.*2524_*2525delinsCG	ENSP00000490268.2:n.*2524_*2525delinsCG
ENST00000585748.3:c.737-186_737-185delinsCG	ENSP00000477641.2:n.737-186_737-185delinsCG
ENST00000585851.2:c.935-186_935-185delinsCG	ENSP00000467912.2:n.935-186_935-185delinsCG
ENST00000326873.12:c.1109-186_1109-185delinsCG MANE Select	ENSP00000324856.6:n.1109-186_1109-185delinsCG
ENST00000326873.11:c.1109-186_1109-185delinsCG	ENSP00000324856.6:n.1109-186_1109-185delinsCG
ENST00000585465.2:n.2656_2657delinsCG
ENST00000586243.5:c.1109-186_1109-185delinsCG	ENSP00000467240.2:n.1109-186_1109-185delinsCG
ENST00000589152.5:n.1807-186_1807-185delinsCG
NM_000455.4:c.1109-186_1109-185delinsCG , LRG_319t1:c.1109-186_1109-185delinsCG	NP_000446.1:n.1109-186_1109-185delinsCG
XM_005259617.1:c.1109-191_1109-190delinsCG	XP_005259674.1:n.1109-191_1109-190delinsCG
XM_011528209.1:c.887-191_887-190delinsCG	XP_011526511.1:n.887-191_887-190delinsCG
XM_005259617.3:c.1109-191_1109-190delinsCG	XP_005259674.1:n.1109-191_1109-190delinsCG
XM_011528209.2:c.887-191_887-190delinsCG	XP_011526511.1:n.887-191_887-190delinsCG
XR_001753738.2:n.1915-186_1915-185delinsCG
XR_001753740.2:n.1885-186_1885-185delinsCG
NM_000455.5:c.1109-186_1109-185delinsCG MANE Select	NP_000446.1:n.1109-186_1109-185delinsCG