Canonical Allele Identifier: CA2317593788

Gene: STK11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1226616_1226617delinsTC , CM000681.2:g.1226616_1226617delinsTC	GRCh38
NC_000019.9:g.1226615_1226616delinsTC , CM000681.1:g.1226615_1226616delinsTC	GRCh37
NC_000019.8:g.1177615_1177616delinsTC	NCBI36
NG_007460.2:g.42210_42211delinsTC , LRG_319:g.42210_42211delinsTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.*2872_*2873delinsTC	ENSP00000490268.2:n.*2872_*2873delinsTC
ENST00000585748.3:c.899_900delinsTC	ENSP00000477641.2:p.Ile300=
ENST00000585851.2:c.1097_1098delinsTC	ENSP00000467912.2:p.Ile366=
ENST00000326873.12:c.1271_1272delinsTC MANE Select	ENSP00000324856.6:p.Ile424=
ENST00000326873.11:c.1271_1272delinsTC	ENSP00000324856.6:p.Ile424=
ENST00000585465.2:n.3004_3005delinsTC
ENST00000586243.5:c.1268_1269delinsTC	ENSP00000467240.2:p.Ile423=
ENST00000589152.5:n.1969_1970delinsTC
NM_000455.4:c.1271_1272delinsTC , LRG_319t1:c.1271_1272delinsTC	NP_000446.1:p.Ile424=
XM_005259617.1:c.1266_1267delinsTC	XP_005259674.1:p.Asp422=
XM_011528209.1:c.1044_1045delinsTC	XP_011526511.1:p.Asp348=
XM_005259617.3:c.1266_1267delinsTC	XP_005259674.1:p.Asp422=
XM_011528209.2:c.1044_1045delinsTC	XP_011526511.1:p.Asp348=
XR_001753738.2:n.2077_2078delinsTC
XR_001753740.2:n.2047_2048delinsTC
NM_000455.5:c.1271_1272delinsTC MANE Select	NP_000446.1:p.Ile424=