Canonical Allele Identifier: CA658684199

Gene: STK11

Linked Data

• ClinVar Variation Id: 492526
• ClinVar RCV Id: RCV000583769
• dbSNP Id: rs1555737841

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1219424_1219425delinsCT , CM000681.2:g.1219424_1219425delinsCT	GRCh38
NC_000019.9:g.1219423_1219424delinsCT , CM000681.1:g.1219423_1219424delinsCT	GRCh37
NC_000019.8:g.1170423_1170424delinsCT	NCBI36
NG_007460.2:g.35018_35019delinsCT , LRG_319:g.35018_35019delinsCT

Transcript Alleles

HGVS	Amino-acid change
ENST00000585465.3:c.464+11_464+12delinsCT	ENSP00000490268.2:n.464+11_464+12delinsCT...
ENST00000585748.3:c.92+11_92+12delinsCT	ENSP00000477641.2:n.92+11_92+12delinsCT
ENST00000585851.2:c.291-949_291-948delinsCT	ENSP00000467912.2:n.291-949_291-948delins...
ENST00000326873.12:c.464+11_464+12delinsCT MANE Select	ENSP00000324856.6:n.464+11_464+12delinsCT...
ENST00000652231.1:c.464+11_464+12delinsCT	ENSP00000498804.1:n.464+11_464+12delinsCT...
ENST00000326873.11:c.464+11_464+12delinsCT	ENSP00000324856.6:n.464+11_464+12delinsCT...
ENST00000585851.1:c.291-949_291-948delinsCT	ENSP00000467912.1:n.291-949_291-948delins...
ENST00000586243.5:c.464+11_464+12delinsCT	ENSP00000467240.2:n.464+11_464+12delinsCT...
ENST00000586358.5:n.287+11_287+12delinsCT
ENST00000589152.5:n.554+11_554+12delinsCT
NM_000455.4:c.464+11_464+12delinsCT , LRG_319t1:c.464+11_464+12delinsCT	NP_000446.1:n.464+11_464+12delinsCT
XM_005259617.1:c.464+11_464+12delinsCT	XP_005259674.1:n.464+11_464+12delinsCT
XM_005259618.3:c.464+11_464+12delinsCT	XP_005259675.1:n.464+11_464+12delinsCT
XM_011528209.1:c.242+11_242+12delinsCT	XP_011526511.1:n.242+11_242+12delinsCT
XR_936204.1:n.1089+11_1089+12delinsCT
XM_005259617.3:c.464+11_464+12delinsCT	XP_005259674.1:n.464+11_464+12delinsCT
XM_011528209.2:c.242+11_242+12delinsCT	XP_011526511.1:n.242+11_242+12delinsCT
XR_001753738.2:n.1089+11_1089+12delinsCT
XR_001753739.1:n.1089+11_1089+12delinsCT
XR_001753740.2:n.1089+11_1089+12delinsCT
NM_000455.5:c.464+11_464+12delinsCT MANE Select	NP_000446.1:n.464+11_464+12delinsCT