Canonical Allele Identifier: CA645369769
Gene: STK11 HGNC NCBI

Linked Data

ClinVar Variation Id: 428791
ClinVar RCV Id: RCV000492673
dbSNP Id: rs1131690952
MyVariant Identifiers: chr19:g.1218498dup (hg19) chr19:g.1218499dup (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1218499dup , CM000681.2:g.1218499dup GRCh38
NC_000019.9:g.1218498dup , CM000681.1:g.1218498dup GRCh37
NC_000019.8:g.1169498dup NCBI36
NG_007460.2:g.34093dup , LRG_319:g.34093dup

Transcript Alleles

HGVS Amino-acid change
ENST00000585465.3:c.373dup ENSP00000490268.2:p.Met125AsnfsTer?
ENST00000585748.3:c.1dup ENSP00000477641.2:p.Met1AsnfsTer?
ENST00000585851.2:c.291-1874dup ENSP00000467912.2:n.291-1874dup
ENST00000326873.12:c.373dup MANE Select ENSP00000324856.6:p.Met125AsnfsTer?
ENST00000652231.1:c.373dup ENSP00000498804.1:p.Met125AsnfsTer?
ENST00000326873.11:c.373dup ENSP00000324856.6:p.Met125AsnfsTer?
ENST00000585748.2:c.1dup ENSP00000477641.1:p.Met1AsnfsTer?
ENST00000585851.1:c.291-1874dup ENSP00000467912.1:n.291-1874dup
ENST00000586243.5:c.373dup ENSP00000467240.2:p.Met125AsnfsTer?
ENST00000586358.5:n.196dup
ENST00000589152.5:n.463dup
ENST00000593219.5:c.*198dup ENSP00000466610.1:n.*198dup
NM_000455.4:c.373dup , LRG_319t1:c.373dup NP_000446.1:p.Met125AsnfsTer?
XM_005259617.1:c.373dup XP_005259674.1:p.Met125AsnfsTer?
XM_005259618.3:c.373dup XP_005259675.1:p.Met125AsnfsTer?
XM_011528209.1:c.151dup XP_011526511.1:p.Met51AsnfsTer?
XR_936204.1:n.998dup
XM_005259617.3:c.373dup XP_005259674.1:p.Met125AsnfsTer?
XM_011528209.2:c.151dup XP_011526511.1:p.Met51AsnfsTer?
XR_001753738.2:n.998dup
XR_001753739.1:n.998dup
XR_001753740.2:n.998dup
NM_000455.5:c.373dup MANE Select NP_000446.1:p.Met125AsnfsTer?
Search 100 bp 5'
Search 100 bp 3'