Canonical Allele Identifier: CA2317581481
Gene: STK11 HGNC NCBI

Linked Data

dbSNP Id: rs1406046777
gnomAD v4: 19-1206849-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1206849C>A , CM000681.2:g.1206849C>A GRCh38
NC_000019.9:g.1206848C>A , CM000681.1:g.1206848C>A GRCh37
NC_000019.8:g.1157848C>A NCBI36
NG_007460.2:g.22443C>A , LRG_319:g.22443C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000585465.3:c.-65C>A ENSP00000490268.2:n.-65C>A
ENST00000585748.3:c.-82-11568C>A ENSP00000477641.2:n.-82-11568C>A
ENST00000326873.12:c.-65C>A MANE Select ENSP00000324856.6:n.-65C>A
ENST00000652231.1:c.-65C>A ENSP00000498804.1:n.-65C>A
ENST00000326873.11:c.-65C>A ENSP00000324856.6:n.-65C>A
ENST00000585748.2:c.-82-11568C>A ENSP00000477641.1:n.-82-11568C>A
ENST00000586243.5:c.-65C>A ENSP00000467240.2:n.-65C>A
ENST00000589152.5:n.26C>A
ENST00000593219.5:c.-65C>A ENSP00000466610.1:n.-65C>A
NM_000455.4:c.-65C>A , LRG_319t1:c.-65C>A NP_000446.1:n.-65C>A
XM_005259617.1:c.-65C>A XP_005259674.1:n.-65C>A
XM_005259618.3:c.-65C>A XP_005259675.1:n.-65C>A
XM_011528209.1:c.-418C>A XP_011526511.1:n.-418C>A
XR_936204.1:n.561C>A
XM_005259617.3:c.-65C>A XP_005259674.1:n.-65C>A
XM_011528209.2:c.-418C>A XP_011526511.1:n.-418C>A
XR_001753738.2:n.561C>A
XR_001753739.1:n.561C>A
XR_001753740.2:n.561C>A
NM_000455.5:c.-65C>A MANE Select NP_000446.1:n.-65C>A