Canonical Allele Identifier: CA645369768
Gene: STK11 HGNC NCBI

Linked Data

ClinVar Variation Id: 428769
ClinVar RCV Id: RCV000492296
dbSNP Id: rs1131690933
MyVariant Identifiers: chr19:g.1218488_1218492dup (hg19) chr19:g.1218489_1218493dup (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1218489_1218493dup , CM000681.2:g.1218489_1218493dup GRCh38
NC_000019.9:g.1218488_1218492dup , CM000681.1:g.1218488_1218492dup GRCh37
NC_000019.8:g.1169488_1169492dup NCBI36
NG_007460.2:g.34083_34087dup , LRG_319:g.34083_34087dup

Transcript Alleles

HGVS Amino-acid change
ENST00000585465.3:c.363_367dup ENSP00000490268.2:p.Gln123ArgfsTer8
ENST00000585748.3:c.-10_-6dup ENSP00000477641.2:n.-10_-6dup
ENST00000585851.2:c.291-1884_291-1880dup ENSP00000467912.2:n.291-1884_291-1880dup
ENST00000326873.12:c.363_367dup MANE Select ENSP00000324856.6:p.Gln123ArgfsTer8
ENST00000652231.1:c.363_367dup ENSP00000498804.1:p.Gln123ArgfsTer8
ENST00000326873.11:c.363_367dup ENSP00000324856.6:p.Gln123ArgfsTer8
ENST00000585748.2:c.-10_-6dup ENSP00000477641.1:n.-10_-6dup
ENST00000585851.1:c.291-1884_291-1880dup ENSP00000467912.1:n.291-1884_291-1880dup
ENST00000586243.5:c.363_367dup ENSP00000467240.2:p.Gln123ArgfsTer8
ENST00000586358.5:n.186_190dup
ENST00000589152.5:n.453_457dup
ENST00000593219.5:c.*188_*192dup ENSP00000466610.1:n.*188_*192dup
NM_000455.4:c.363_367dup , LRG_319t1:c.363_367dup NP_000446.1:p.Gln123ArgfsTer8
XM_005259617.1:c.363_367dup XP_005259674.1:p.Gln123ArgfsTer8
XM_005259618.3:c.363_367dup XP_005259675.1:p.Gln123ArgfsTer8
XM_011528209.1:c.141_145dup XP_011526511.1:p.Gln49ArgfsTer8
XR_936204.1:n.988_992dup
XM_005259617.3:c.363_367dup XP_005259674.1:p.Gln123ArgfsTer8
XM_011528209.2:c.141_145dup XP_011526511.1:p.Gln49ArgfsTer8
XR_001753738.2:n.988_992dup
XR_001753739.1:n.988_992dup
XR_001753740.2:n.988_992dup
NM_000455.5:c.363_367dup MANE Select NP_000446.1:p.Gln123ArgfsTer8
Search 100 bp 5'
Search 100 bp 3'