Canonical Allele Identifier: CA2735567020
Gene: STK11 HGNC NCBI

Linked Data

dbSNP Id: rs2145436441

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1226597_1226598del , CM000681.2:g.1226597_1226598del GRCh38
NC_000019.9:g.1226596_1226597del , CM000681.1:g.1226596_1226597del GRCh37
NC_000019.8:g.1177596_1177597del NCBI36
NG_007460.2:g.42191_42192del , LRG_319:g.42191_42192del

Transcript Alleles

HGVS Amino-acid Change
ENST00000585465.3:c.*2853_*2854del ENSP00000490268.2:n.*2853_*2854del
ENST00000585748.3:c.880_881del ENSP00000477641.2:p.Cys294LeufsTer?
ENST00000585851.2:c.1078_1079del ENSP00000467912.2:p.Cys360LeufsTer?
ENST00000326873.12:c.1252_1253del MANE Select ENSP00000324856.6:p.Cys418LeufsTer?
ENST00000326873.11:c.1252_1253del ENSP00000324856.6:p.Cys418LeufsTer?
ENST00000585465.2:n.2985_2986del
ENST00000586243.5:c.1251_1252del ENSP00000467240.2:p.Ala418CysfsTer?
ENST00000589152.5:n.1950_1951del
NM_000455.4:c.1252_1253del , LRG_319t1:c.1252_1253del NP_000446.1:p.Cys418LeufsTer?
XM_005259617.1:c.1247_1248del XP_005259674.1:p.Leu416ProfsTer?
XM_011528209.1:c.1025_1026del XP_011526511.1:p.Leu342ProfsTer?
XM_005259617.3:c.1247_1248del XP_005259674.1:p.Leu416ProfsTer?
XM_011528209.2:c.1025_1026del XP_011526511.1:p.Leu342ProfsTer?
XR_001753738.2:n.2058_2059del
XR_001753740.2:n.2028_2029del
NM_000455.5:c.1252_1253del MANE Select NP_000446.1:p.Cys418LeufsTer?