Canonical Allele Identifier: CA645369770
Gene: STK11 HGNC NCBI

Linked Data

ClinVar Variation Id: 428782
ClinVar RCV Id: RCV000492160
dbSNP Id: rs1131690946
MyVariant Identifiers: chr19:g.1220590dup (hg19) chr19:g.1220591dup (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1220591dup , CM000681.2:g.1220591dup GRCh38
NC_000019.9:g.1220590dup , CM000681.1:g.1220590dup GRCh37
NC_000019.8:g.1171590dup NCBI36
NG_007460.2:g.36185dup , LRG_319:g.36185dup

Transcript Alleles

HGVS Amino-acid change
ENST00000585465.3:c.608dup ENSP00000490268.2:p.Phe204ValfsTer?
ENST00000585748.3:c.236dup ENSP00000477641.2:p.Phe80ValfsTer?
ENST00000585851.2:c.434dup ENSP00000467912.2:p.Phe146ValfsTer?
ENST00000326873.12:c.608dup MANE Select ENSP00000324856.6:p.Phe204ValfsTer?
ENST00000652231.1:c.608dup ENSP00000498804.1:p.Phe204ValfsTer?
ENST00000326873.11:c.608dup ENSP00000324856.6:p.Phe204ValfsTer?
ENST00000585851.1:c.434dup ENSP00000467912.1:p.Phe146ValfsTer?
ENST00000586243.5:c.608dup ENSP00000467240.2:p.Phe204ValfsTer?
ENST00000586358.5:n.506dup
ENST00000589152.5:n.698dup
ENST00000591133.2:n.579dup
NM_000455.4:c.608dup , LRG_319t1:c.608dup NP_000446.1:p.Phe204ValfsTer?
XM_005259617.1:c.608dup XP_005259674.1:p.Phe204ValfsTer?
XM_005259618.3:c.608dup XP_005259675.1:p.Phe204ValfsTer?
XM_011528209.1:c.386dup XP_011526511.1:p.Phe130ValfsTer?
XR_936204.1:n.1233dup
XM_005259617.3:c.608dup XP_005259674.1:p.Phe204ValfsTer?
XM_011528209.2:c.386dup XP_011526511.1:p.Phe130ValfsTer?
XR_001753738.2:n.1233dup
XR_001753739.1:n.1233dup
XR_001753740.2:n.1233dup
NM_000455.5:c.608dup MANE Select NP_000446.1:p.Phe204ValfsTer?
Search 100 bp 5'
Search 100 bp 3'