Canonical Allele Identifier: CA2317581409
Gene: STK11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1206759A= , CM000681.2:g.1206759A= GRCh38
NC_000019.9:g.1206758A= , CM000681.1:g.1206758A= GRCh37
NC_000019.8:g.1157758A= NCBI36
NG_007460.2:g.22353A= , LRG_319:g.22353A=

Transcript Alleles

HGVS Amino-acid change
ENST00000585465.3:c.-155A= ENSP00000490268.2:n.-155A=
ENST00000585748.3:c.-82-11658A= ENSP00000477641.2:n.-82-11658A=
ENST00000326873.12:c.-155A= MANE Select ENSP00000324856.6:n.-155A=
ENST00000652231.1:c.-155A= ENSP00000498804.1:n.-155A=
ENST00000326873.11:c.-155A= ENSP00000324856.6:n.-155A=
ENST00000585748.2:c.-82-11658A= ENSP00000477641.1:n.-82-11658A=
ENST00000586243.5:c.-155A= ENSP00000467240.2:n.-155A=
NM_000455.4:c.-155A= , LRG_319t1:c.-155A= NP_000446.1:n.-155A=
XM_005259617.1:c.-155A= XP_005259674.1:n.-155A=
XM_005259618.3:c.-155A= XP_005259675.1:n.-155A=
XM_011528209.1:c.-508A= XP_011526511.1:n.-508A=
XR_936204.1:n.471A=
XM_005259617.3:c.-155A= XP_005259674.1:n.-155A=
XM_011528209.2:c.-508A= XP_011526511.1:n.-508A=
XR_001753738.2:n.471A=
XR_001753739.1:n.471A=
XR_001753740.2:n.471A=
NM_000455.5:c.-155A= MANE Select NP_000446.1:n.-155A=