Canonical Allele Identifier: CA2317581408
Gene: STK11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1206757G= , CM000681.2:g.1206757G= GRCh38
NC_000019.9:g.1206756G= , CM000681.1:g.1206756G= GRCh37
NC_000019.8:g.1157756G= NCBI36
NG_007460.2:g.22351G= , LRG_319:g.22351G=

Transcript Alleles

HGVS Amino-acid change
ENST00000585465.3:c.-157G= ENSP00000490268.2:n.-157G=
ENST00000585748.3:c.-82-11660G= ENSP00000477641.2:n.-82-11660G=
ENST00000326873.12:c.-157G= MANE Select ENSP00000324856.6:n.-157G=
ENST00000652231.1:c.-157G= ENSP00000498804.1:n.-157G=
ENST00000326873.11:c.-157G= ENSP00000324856.6:n.-157G=
ENST00000585748.2:c.-82-11660G= ENSP00000477641.1:n.-82-11660G=
ENST00000586243.5:c.-157G= ENSP00000467240.2:n.-157G=
NM_000455.4:c.-157G= , LRG_319t1:c.-157G= NP_000446.1:n.-157G=
XM_005259617.1:c.-157G= XP_005259674.1:n.-157G=
XM_005259618.3:c.-157G= XP_005259675.1:n.-157G=
XM_011528209.1:c.-510G= XP_011526511.1:n.-510G=
XR_936204.1:n.469G=
XM_005259617.3:c.-157G= XP_005259674.1:n.-157G=
XM_011528209.2:c.-510G= XP_011526511.1:n.-510G=
XR_001753738.2:n.469G=
XR_001753739.1:n.469G=
XR_001753740.2:n.469G=
NM_000455.5:c.-157G= MANE Select NP_000446.1:n.-157G=