Canonical Allele Identifier: CA915951604

Gene: STK11

Linked Data

• ClinVar Variation Id: 797961
• ClinVar RCV Id: RCV000981453
• dbSNP Id: rs1599932274

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1226542_1226543delinsAT , CM000681.2:g.1226542_1226543delinsAT	GRCh38
NC_000019.9:g.1226541_1226542delinsAT , CM000681.1:g.1226541_1226542delinsAT	GRCh37
NC_000019.8:g.1177541_1177542delinsAT	NCBI36
NG_007460.2:g.42136_42137delinsAT , LRG_319:g.42136_42137delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.*2798_*2799delinsAT	ENSP00000490268.2:n.*2798_*2799delinsAT
ENST00000585748.3:c.825_826delinsAT	ENSP00000477641.2:p.Gln275=
ENST00000585851.2:c.1023_1024delinsAT	ENSP00000467912.2:p.Gln341=
ENST00000326873.12:c.1197_1198delinsAT MANE Select	ENSP00000324856.6:p.Gln399=
ENST00000326873.11:c.1197_1198delinsAT	ENSP00000324856.6:p.Gln399=
ENST00000585465.2:n.2930_2931delinsAT
ENST00000586243.5:c.1197_1198delinsAT	ENSP00000467240.2:p.Gln399=
ENST00000589152.5:n.1895_1896delinsAT
NM_000455.4:c.1197_1198delinsAT , LRG_319t1:c.1197_1198delinsAT	NP_000446.1:p.Gln399=
XM_005259617.1:c.1192_1193delinsAT	XP_005259674.1:p.Ala398Ile
XM_011528209.1:c.970_971delinsAT	XP_011526511.1:p.Ala324Ile
XM_005259617.3:c.1192_1193delinsAT	XP_005259674.1:p.Ala398Ile
XM_011528209.2:c.970_971delinsAT	XP_011526511.1:p.Ala324Ile
XR_001753738.2:n.2003_2004delinsAT
XR_001753740.2:n.1973_1974delinsAT
NM_000455.5:c.1197_1198delinsAT MANE Select	NP_000446.1:p.Gln399=