Canonical Allele Identifier: CA2317581480
Gene: STK11 HGNC NCBI

Genomic Alleles

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

Transcript Alleles

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