Canonical Allele Identifier: CA16620760

Gene: STK11

Linked Data

• ClinVar Variation Id: 422018
• ClinVar RCV Id: RCV000481685
• dbSNP Id: rs1064795504

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1226616_1226617delinsAG , CM000681.2:g.1226616_1226617delinsAG	GRCh38
NC_000019.9:g.1226615_1226616delinsAG , CM000681.1:g.1226615_1226616delinsAG	GRCh37
NC_000019.8:g.1177615_1177616delinsAG	NCBI36
NG_007460.2:g.42210_42211delinsAG , LRG_319:g.42210_42211delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.*2872_*2873delinsAG	ENSP00000490268.2:n.*2872_*2873delinsAG
ENST00000585748.3:c.899_900delinsAG	ENSP00000477641.2:p.Ile300Lys
ENST00000585851.2:c.1097_1098delinsAG	ENSP00000467912.2:p.Ile366Lys
ENST00000326873.12:c.1271_1272delinsAG MANE Select	ENSP00000324856.6:p.Ile424Lys
ENST00000326873.11:c.1271_1272delinsAG	ENSP00000324856.6:p.Ile424Lys
ENST00000585465.2:n.3004_3005delinsAG
ENST00000586243.5:c.1268_1269delinsAG	ENSP00000467240.2:p.Ile423Lys
ENST00000589152.5:n.1969_1970delinsAG
NM_000455.4:c.1271_1272delinsAG , LRG_319t1:c.1271_1272delinsAG	NP_000446.1:p.Ile424Lys
XM_005259617.1:c.1266_1267delinsAG	XP_005259674.1:p.Asp422_Pro423delinsGluAla
XM_011528209.1:c.1044_1045delinsAG	XP_011526511.1:p.Asp348_Pro349delinsGluAla
XM_005259617.3:c.1266_1267delinsAG	XP_005259674.1:p.Asp422_Pro423delinsGluAla
XM_011528209.2:c.1044_1045delinsAG	XP_011526511.1:p.Asp348_Pro349delinsGluAla
XR_001753738.2:n.2077_2078delinsAG
XR_001753740.2:n.2047_2048delinsAG
NM_000455.5:c.1271_1272delinsAG MANE Select	NP_000446.1:p.Ile424Lys