Canonical Allele Identifier: CA402948846
Gene: STK11 HGNC NCBI

Linked Data

gnomAD v4: 19-1220394-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1220394C>A , CM000681.2:g.1220394C>A GRCh38
NC_000019.9:g.1220393C>A , CM000681.1:g.1220393C>A GRCh37
NC_000019.8:g.1171393C>A NCBI36
NG_007460.2:g.35988C>A , LRG_319:g.35988C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000585465.3:c.486C>A ENSP00000490268.2:p.Asp162Glu
ENST00000585748.3:c.114C>A ENSP00000477641.2:p.Asp38Glu
ENST00000585851.2:c.312C>A ENSP00000467912.2:p.Asp104Glu
ENST00000326873.12:c.486C>A MANE Select ENSP00000324856.6:p.Asp162Glu
ENST00000652231.1:c.486C>A ENSP00000498804.1:p.Asp162Glu
ENST00000326873.11:c.486C>A ENSP00000324856.6:p.Asp162Glu
ENST00000585851.1:c.312C>A ENSP00000467912.1:p.Asp104Glu
ENST00000586243.5:c.486C>A ENSP00000467240.2:p.Asp162Glu
ENST00000586358.5:n.309C>A
ENST00000589152.5:n.576C>A
ENST00000591133.2:n.382C>A
NM_000455.4:c.486C>A , LRG_319t1:c.486C>A NP_000446.1:p.Asp162Glu
XM_005259617.1:c.486C>A XP_005259674.1:p.Asp162Glu
XM_005259618.3:c.486C>A XP_005259675.1:p.Asp162Glu
XM_011528209.1:c.264C>A XP_011526511.1:p.Asp88Glu
XR_936204.1:n.1111C>A
XM_005259617.3:c.486C>A XP_005259674.1:p.Asp162Glu
XM_011528209.2:c.264C>A XP_011526511.1:p.Asp88Glu
XR_001753738.2:n.1111C>A
XR_001753739.1:n.1111C>A
XR_001753740.2:n.1111C>A
NM_000455.5:c.486C>A MANE Select NP_000446.1:p.Asp162Glu