Canonical Allele Identifier: CA645369767
Gene: STK11 HGNC NCBI

Linked Data

ClinVar Variation Id: 428765
ClinVar RCV Id: RCV000492465
dbSNP Id: rs1131690929
MyVariant Identifiers: chr19:g.1207121dup (hg19) chr19:g.1207122dup (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1207122dup , CM000681.2:g.1207122dup GRCh38
NC_000019.9:g.1207121dup , CM000681.1:g.1207121dup GRCh37
NC_000019.8:g.1158121dup NCBI36
NG_007460.2:g.22716dup , LRG_319:g.22716dup

Transcript Alleles

HGVS Amino-acid change
ENST00000585465.3:c.209dup ENSP00000490268.2:p.Thr71AspfsTer?
ENST00000585748.3:c.-82-11295dup ENSP00000477641.2:n.-82-11295dup
ENST00000585851.2:c.209dup ENSP00000467912.2:p.Thr71AspfsTer?
ENST00000326873.12:c.209dup MANE Select ENSP00000324856.6:p.Thr71AspfsTer?
ENST00000652231.1:c.209dup ENSP00000498804.1:p.Thr71AspfsTer?
ENST00000326873.11:c.209dup ENSP00000324856.6:p.Thr71AspfsTer?
ENST00000585748.2:c.-82-11295dup ENSP00000477641.1:n.-82-11295dup
ENST00000585851.1:c.209dup ENSP00000467912.1:p.Thr71AspfsTer?
ENST00000586243.5:c.209dup ENSP00000467240.2:p.Thr71AspfsTer?
ENST00000586358.5:n.32dup
ENST00000589152.5:n.299dup
ENST00000593219.5:c.209dup ENSP00000466610.1:p.Thr71AspfsTer?
NM_000455.4:c.209dup , LRG_319t1:c.209dup NP_000446.1:p.Thr71AspfsTer?
XM_005259617.1:c.209dup XP_005259674.1:p.Thr71AspfsTer?
XM_005259618.3:c.209dup XP_005259675.1:p.Thr71AspfsTer?
XM_011528209.1:c.-145dup XP_011526511.1:n.-145dup
XR_936204.1:n.834dup
XM_005259617.3:c.209dup XP_005259674.1:p.Thr71AspfsTer?
XM_011528209.2:c.-145dup XP_011526511.1:n.-145dup
XR_001753738.2:n.834dup
XR_001753739.1:n.834dup
XR_001753740.2:n.834dup
NM_000455.5:c.209dup MANE Select NP_000446.1:p.Thr71AspfsTer?
Search 100 bp 5'
Search 100 bp 3'