Canonical Allele Identifier: CA16620754
Gene: STK11 HGNC NCBI

Linked Data

ClinVar Variation Id: 418779
ClinVar RCV Id: RCV000487243 RCV001865435 RCV002374885
dbSNP Id: rs1064793427
MyVariant Identifiers: chr19:g.1221995del (hg19) chr19:g.1221996del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1221996del , CM000681.2:g.1221996del GRCh38
NC_000019.9:g.1221995del , CM000681.1:g.1221995del GRCh37
NC_000019.8:g.1172995del NCBI36
NG_007460.2:g.37590del , LRG_319:g.37590del

Transcript Alleles

HGVS Amino-acid change
ENST00000585465.3:c.910del ENSP00000490268.2:p.Arg304GlyfsTer?
ENST00000585748.3:c.538del ENSP00000477641.2:p.Arg180GlyfsTer?
ENST00000585851.2:c.736del ENSP00000467912.2:p.Arg246GlyfsTer?
ENST00000326873.12:c.910del MANE Select ENSP00000324856.6:p.Arg304GlyfsTer?
ENST00000652231.1:c.910del ENSP00000498804.1:p.Arg304GlyfsTer?
ENST00000326873.11:c.910del ENSP00000324856.6:p.Arg304GlyfsTer?
ENST00000586243.5:c.910del ENSP00000467240.2:p.Arg304GlyfsTer?
ENST00000589152.5:n.1608del
ENST00000591133.2:n.881del
NM_000455.4:c.910del , LRG_319t1:c.910del NP_000446.1:p.Arg304GlyfsTer?
XM_005259617.1:c.910del XP_005259674.1:p.Arg304GlyfsTer?
XM_005259618.3:c.910del XP_005259675.1:p.Arg304GlyfsTer?
XM_011528209.1:c.688del XP_011526511.1:p.Arg230GlyfsTer?
XR_936204.1:n.1686del
XM_005259617.3:c.910del XP_005259674.1:p.Arg304GlyfsTer?
XM_011528209.2:c.688del XP_011526511.1:p.Arg230GlyfsTer?
XR_001753738.2:n.1716del
XR_001753739.1:n.1716del
XR_001753740.2:n.1686del
NM_000455.5:c.910del MANE Select NP_000446.1:p.Arg304GlyfsTer?
Search 100 bp 5'
Search 100 bp 3'