Canonical Allele Identifier: CA16616228
Gene: STK11 HGNC NCBI

Linked Data

ClinVar Variation Id: 403776
ClinVar RCV Id: RCV000464957
dbSNP Id: rs1060499960
MyVariant Identifiers: chr19:g.1223052_1223059del (hg19) chr19:g.1223053_1223060del (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1223053_1223060del , CM000681.2:g.1223053_1223060del GRCh38
NC_000019.9:g.1223052_1223059del , CM000681.1:g.1223052_1223059del GRCh37
NC_000019.8:g.1174052_1174059del NCBI36
NG_007460.2:g.38647_38654del , LRG_319:g.38647_38654del

Transcript Alleles

HGVS Amino-acid change
ENST00000585465.3:c.989_996del ENSP00000490268.2:p.Asp330AlafsTer27
ENST00000585748.3:c.617_624del ENSP00000477641.2:p.Asp206AlafsTer27
ENST00000585851.2:c.815_822del ENSP00000467912.2:p.Asp272AlafsTer27
ENST00000326873.12:c.989_996del MANE Select ENSP00000324856.6:p.Asp330AlafsTer27
ENST00000652231.1:c.989_996del ENSP00000498804.1:p.Asp330AlafsTer27
ENST00000326873.11:c.989_996del ENSP00000324856.6:p.Asp330AlafsTer27
ENST00000586243.5:c.989_996del ENSP00000467240.2:p.Asp330AlafsTer27
ENST00000589152.5:n.1687_1694del
ENST00000591133.2:n.960_967del
NM_000455.4:c.989_996del , LRG_319t1:c.989_996del NP_000446.1:p.Asp330AlafsTer27
XM_005259617.1:c.989_996del XP_005259674.1:p.Asp330AlafsTer27
XM_005259618.3:c.989_996del XP_005259675.1:p.Asp330AlafsTer27
XM_011528209.1:c.767_774del XP_011526511.1:p.Asp256AlafsTer27
XR_936204.1:n.1765_1772del
XM_005259617.3:c.989_996del XP_005259674.1:p.Asp330AlafsTer27
XM_011528209.2:c.767_774del XP_011526511.1:p.Asp256AlafsTer27
XR_001753738.2:n.1795_1802del
XR_001753739.1:n.1795_1802del
XR_001753740.2:n.1765_1772del
NM_000455.5:c.989_996del MANE Select NP_000446.1:p.Asp330AlafsTer27
Search 100 bp 5'
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