Canonical Allele Identifier: CA2580096140
Gene: STK11 HGNC NCBI

Linked Data

ClinVar Variation Id: 1776678
ClinVar RCV Id: RCV002401136

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1223068_1223083dup , CM000681.2:g.1223068_1223083dup GRCh38
NC_000019.9:g.1223067_1223082dup , CM000681.1:g.1223067_1223082dup GRCh37
NC_000019.8:g.1174067_1174082dup NCBI36
NG_007460.2:g.38662_38677dup , LRG_319:g.38662_38677dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000585465.3:c.1004_1019dup ENSP00000490268.2:p.Leu341AspfsTer24
ENST00000585748.3:c.632_647dup ENSP00000477641.2:p.Leu217AspfsTer24
ENST00000585851.2:c.830_845dup ENSP00000467912.2:p.Leu283AspfsTer24
ENST00000326873.12:c.1004_1019dup MANE Select ENSP00000324856.6:p.Leu341AspfsTer24
ENST00000652231.1:c.1004_1019dup ENSP00000498804.1:p.Leu341AspfsTer24
ENST00000326873.11:c.1004_1019dup ENSP00000324856.6:p.Leu341AspfsTer24
ENST00000586243.5:c.1004_1019dup ENSP00000467240.2:p.Leu341AspfsTer24
ENST00000589152.5:n.1702_1717dup
ENST00000591133.2:n.975_990dup
NM_000455.4:c.1004_1019dup , LRG_319t1:c.1004_1019dup NP_000446.1:p.Leu341AspfsTer24
XM_005259617.1:c.1004_1019dup XP_005259674.1:p.Leu341AspfsTer24
XM_005259618.3:c.1004_1019dup XP_005259675.1:p.Leu341AspfsTer24
XM_011528209.1:c.782_797dup XP_011526511.1:p.Leu267AspfsTer24
XR_936204.1:n.1780_1795dup
XM_005259617.3:c.1004_1019dup XP_005259674.1:p.Leu341AspfsTer24
XM_011528209.2:c.782_797dup XP_011526511.1:p.Leu267AspfsTer24
XR_001753738.2:n.1810_1825dup
XR_001753739.1:n.1810_1825dup
XR_001753740.2:n.1780_1795dup
NM_000455.5:c.1004_1019dup MANE Select NP_000446.1:p.Leu341AspfsTer24