Canonical Allele Identifier: CA2695227893
Gene: STK11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1220393_1220396dup , CM000681.2:g.1220393_1220396dup GRCh38
NC_000019.9:g.1220392_1220395dup , CM000681.1:g.1220392_1220395dup GRCh37
NC_000019.8:g.1171392_1171395dup NCBI36
NG_007460.2:g.35987_35990dup , LRG_319:g.35987_35990dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000585465.3:c.485_488dup ENSP00000490268.2:p.Leu164ArgfsTer7
ENST00000585748.3:c.113_116dup ENSP00000477641.2:p.Leu40ArgfsTer7
ENST00000585851.2:c.311_314dup ENSP00000467912.2:p.Leu106ArgfsTer7
ENST00000326873.12:c.485_488dup MANE Select ENSP00000324856.6:p.Leu164ArgfsTer7
ENST00000652231.1:c.485_488dup ENSP00000498804.1:p.Leu164ArgfsTer7
ENST00000326873.11:c.485_488dup ENSP00000324856.6:p.Leu164ArgfsTer7
ENST00000585851.1:c.311_314dup ENSP00000467912.1:p.Leu106ArgfsTer7
ENST00000586243.5:c.485_488dup ENSP00000467240.2:p.Leu164ArgfsTer7
ENST00000586358.5:n.308_311dup
ENST00000589152.5:n.575_578dup
ENST00000591133.2:n.381_384dup
NM_000455.4:c.485_488dup , LRG_319t1:c.485_488dup NP_000446.1:p.Leu164ArgfsTer7
XM_005259617.1:c.485_488dup XP_005259674.1:p.Leu164ArgfsTer7
XM_005259618.3:c.485_488dup XP_005259675.1:p.Leu164ArgfsTer7
XM_011528209.1:c.263_266dup XP_011526511.1:p.Leu90ArgfsTer7
XR_936204.1:n.1110_1113dup
XM_005259617.3:c.485_488dup XP_005259674.1:p.Leu164ArgfsTer7
XM_011528209.2:c.263_266dup XP_011526511.1:p.Leu90ArgfsTer7
XR_001753738.2:n.1110_1113dup
XR_001753739.1:n.1110_1113dup
XR_001753740.2:n.1110_1113dup
NM_000455.5:c.485_488dup MANE Select NP_000446.1:p.Leu164ArgfsTer7