Canonical Allele Identifier: CA402951538
Gene: STK11 HGNC NCBI

Linked Data

gnomAD v4: 19-1223022-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1223022G>A , CM000681.2:g.1223022G>A GRCh38
NC_000019.9:g.1223021G>A , CM000681.1:g.1223021G>A GRCh37
NC_000019.8:g.1174021G>A NCBI36
NG_007460.2:g.38616G>A , LRG_319:g.38616G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000585465.3:c.958G>A ENSP00000490268.2:p.Val320Met
ENST00000585748.3:c.586G>A ENSP00000477641.2:p.Val196Met
ENST00000585851.2:c.784G>A ENSP00000467912.2:p.Val262Met
ENST00000326873.12:c.958G>A MANE Select ENSP00000324856.6:p.Val320Met
ENST00000652231.1:c.958G>A ENSP00000498804.1:p.Val320Met
ENST00000326873.11:c.958G>A ENSP00000324856.6:p.Val320Met
ENST00000586243.5:c.958G>A ENSP00000467240.2:p.Val320Met
ENST00000589152.5:n.1656G>A
ENST00000591133.2:n.929G>A
NM_000455.4:c.958G>A , LRG_319t1:c.958G>A NP_000446.1:p.Val320Met
XM_005259617.1:c.958G>A XP_005259674.1:p.Val320Met
XM_005259618.3:c.958G>A XP_005259675.1:p.Val320Met
XM_011528209.1:c.736G>A XP_011526511.1:p.Val246Met
XR_936204.1:n.1734G>A
XM_005259617.3:c.958G>A XP_005259674.1:p.Val320Met
XM_011528209.2:c.736G>A XP_011526511.1:p.Val246Met
XR_001753738.2:n.1764G>A
XR_001753739.1:n.1764G>A
XR_001753740.2:n.1734G>A
NM_000455.5:c.958G>A MANE Select NP_000446.1:p.Val320Met