Canonical Allele Identifier: CA402954013
Gene: STK11 HGNC NCBI

Linked Data

dbSNP Id: rs1459406168
gnomAD v4: 19-1226593-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1226593G>T , CM000681.2:g.1226593G>T GRCh38
NC_000019.9:g.1226592G>T , CM000681.1:g.1226592G>T GRCh37
NC_000019.8:g.1177592G>T NCBI36
NG_007460.2:g.42187G>T , LRG_319:g.42187G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000585465.3:c.*2849G>T ENSP00000490268.2:n.*2849G>T
ENST00000585748.3:c.876G>T ENSP00000477641.2:p.Lys292Asn
ENST00000585851.2:c.1074G>T ENSP00000467912.2:p.Lys358Asn
ENST00000326873.12:c.1248G>T MANE Select ENSP00000324856.6:p.Lys416Asn
ENST00000326873.11:c.1248G>T ENSP00000324856.6:p.Lys416Asn
ENST00000585465.2:n.2981G>T
ENST00000586243.5:c.1247G>T ENSP00000467240.2:p.Arg416Met
ENST00000589152.5:n.1946G>T
NM_000455.4:c.1248G>T , LRG_319t1:c.1248G>T NP_000446.1:p.Lys416Asn
XM_005259617.1:c.1243G>T XP_005259674.1:p.Gly415Cys
XM_011528209.1:c.1021G>T XP_011526511.1:p.Gly341Cys
XM_005259617.3:c.1243G>T XP_005259674.1:p.Gly415Cys
XM_011528209.2:c.1021G>T XP_011526511.1:p.Gly341Cys
XR_001753738.2:n.2054G>T
XR_001753740.2:n.2024G>T
NM_000455.5:c.1248G>T MANE Select NP_000446.1:p.Lys416Asn