Canonical Allele Identifier: CA2740091837

Gene: STK11

Linked Data

• ClinVar Variation Id: 3010206
• ClinVar RCV Id: RCV003867381

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1223025_1223026delinsT , CM000681.2:g.1223025_1223026delinsT	GRCh38
NC_000019.9:g.1223024_1223025delinsT , CM000681.1:g.1223024_1223025delinsT	GRCh37
NC_000019.8:g.1174024_1174025delinsT	NCBI36
NG_007460.2:g.38619_38620delinsT , LRG_319:g.38619_38620delinsT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.961_962delinsT	ENSP00000490268.2:p.Pro321SerfsTer15
ENST00000585748.3:c.589_590delinsT	ENSP00000477641.2:p.Pro197SerfsTer15
ENST00000585851.2:c.787_788delinsT	ENSP00000467912.2:p.Pro263SerfsTer15
ENST00000326873.12:c.961_962delinsT MANE Select	ENSP00000324856.6:p.Pro321SerfsTer15
ENST00000652231.1:c.961_962delinsT	ENSP00000498804.1:p.Pro321SerfsTer15
ENST00000326873.11:c.961_962delinsT	ENSP00000324856.6:p.Pro321SerfsTer15
ENST00000586243.5:c.961_962delinsT	ENSP00000467240.2:p.Pro321SerfsTer15
ENST00000589152.5:n.1659_1660delinsT
ENST00000591133.2:n.932_933delinsT
NM_000455.4:c.961_962delinsT , LRG_319t1:c.961_962delinsT	NP_000446.1:p.Pro321SerfsTer15
XM_005259617.1:c.961_962delinsT	XP_005259674.1:p.Pro321SerfsTer15
XM_005259618.3:c.961_962delinsT	XP_005259675.1:p.Pro321SerfsTer15
XM_011528209.1:c.739_740delinsT	XP_011526511.1:p.Pro247SerfsTer15
XR_936204.1:n.1737_1738delinsT
XM_005259617.3:c.961_962delinsT	XP_005259674.1:p.Pro321SerfsTer15
XM_011528209.2:c.739_740delinsT	XP_011526511.1:p.Pro247SerfsTer15
XR_001753738.2:n.1767_1768delinsT
XR_001753739.1:n.1767_1768delinsT
XR_001753740.2:n.1737_1738delinsT
NM_000455.5:c.961_962delinsT MANE Select	NP_000446.1:p.Pro321SerfsTer15