Canonical Allele Identifier: CA16043550
Gene: STK11 HGNC NCBI

Linked Data

dbSNP Id: rs1057518830
MyVariant Identifiers: chr19:g.1221333_1221335del (hg19) chr19:g.1221334_1221336del (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1221334_1221336del , CM000681.2:g.1221334_1221336del GRCh38
NC_000019.9:g.1221333_1221335del , CM000681.1:g.1221333_1221335del GRCh37
NC_000019.8:g.1172333_1172335del NCBI36
NG_007460.2:g.36928_36930del , LRG_319:g.36928_36930del

Transcript Alleles

HGVS Amino-acid change
ENST00000585465.3:c.856_858del ENSP00000490268.2:p.Leu286del
ENST00000585748.3:c.484_486del ENSP00000477641.2:p.Leu162del
ENST00000585851.2:c.682_684del ENSP00000467912.2:p.Leu228del
ENST00000326873.12:c.856_858del MANE Select ENSP00000324856.6:p.Leu286del
ENST00000652231.1:c.856_858del ENSP00000498804.1:p.Leu286del
ENST00000326873.11:c.856_858del ENSP00000324856.6:p.Leu286del
ENST00000586243.5:c.856_858del ENSP00000467240.2:p.Leu286del
ENST00000586358.5:n.754_756del
ENST00000589152.5:n.946_948del
ENST00000591133.2:n.827_829del
NM_000455.4:c.856_858del , LRG_319t1:c.856_858del NP_000446.1:p.Leu286del
XM_005259617.1:c.856_858del XP_005259674.1:p.Leu286del
XM_005259618.3:c.856_858del XP_005259675.1:p.Leu286del
XM_011528209.1:c.634_636del XP_011526511.1:p.Leu212del
XR_936204.1:n.1481_1483del
XM_005259617.3:c.856_858del XP_005259674.1:p.Leu286del
XM_011528209.2:c.634_636del XP_011526511.1:p.Leu212del
XR_001753738.2:n.1481_1483del
XR_001753739.1:n.1481_1483del
XR_001753740.2:n.1481_1483del
NM_000455.5:c.856_858del MANE Select NP_000446.1:p.Leu286del
Search 100 bp 5'
Search 100 bp 3'