Canonical Allele Identifier: CA645369779
Gene: STK11 HGNC NCBI

Linked Data

ClinVar Variation Id: 428786
ClinVar RCV Id: RCV000492368 RCV000990129
dbSNP Id: rs1131690949
MyVariant Identifiers: chr19:g.1221320dup (hg19) chr19:g.1221321dup (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1221321dup , CM000681.2:g.1221321dup GRCh38
NC_000019.9:g.1221320dup , CM000681.1:g.1221320dup GRCh37
NC_000019.8:g.1172320dup NCBI36
NG_007460.2:g.36915dup , LRG_319:g.36915dup

Transcript Alleles

HGVS Amino-acid change
ENST00000585465.3:c.843dup ENSP00000490268.2:p.Leu282AlafsTer3
ENST00000585748.3:c.471dup ENSP00000477641.2:p.Leu158AlafsTer3
ENST00000585851.2:c.669dup ENSP00000467912.2:p.Leu224AlafsTer3
ENST00000326873.12:c.843dup MANE Select ENSP00000324856.6:p.Leu282AlafsTer3
ENST00000652231.1:c.843dup ENSP00000498804.1:p.Leu282AlafsTer3
ENST00000326873.11:c.843dup ENSP00000324856.6:p.Leu282AlafsTer3
ENST00000586243.5:c.843dup ENSP00000467240.2:p.Leu282AlafsTer3
ENST00000586358.5:n.741dup
ENST00000589152.5:n.933dup
ENST00000591133.2:n.814dup
NM_000455.4:c.843dup , LRG_319t1:c.843dup NP_000446.1:p.Leu282AlafsTer3
XM_005259617.1:c.843dup XP_005259674.1:p.Leu282AlafsTer3
XM_005259618.3:c.843dup XP_005259675.1:p.Leu282AlafsTer3
XM_011528209.1:c.621dup XP_011526511.1:p.Leu208AlafsTer3
XR_936204.1:n.1468dup
XM_005259617.3:c.843dup XP_005259674.1:p.Leu282AlafsTer3
XM_011528209.2:c.621dup XP_011526511.1:p.Leu208AlafsTer3
XR_001753738.2:n.1468dup
XR_001753739.1:n.1468dup
XR_001753740.2:n.1468dup
NM_000455.5:c.843dup MANE Select NP_000446.1:p.Leu282AlafsTer3
Search 100 bp 5'
Search 100 bp 3'