Canonical Allele Identifier: CA2317581445

Gene: STK11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1206801_1206808delinsTTTTTTTC , CM000681.2:g.1206801_1206808delinsTTTTTTTC	GRCh38
NC_000019.9:g.1206800_1206807delinsTTTTTTTC , CM000681.1:g.1206800_1206807delinsTTTTTTTC	GRCh37
NC_000019.8:g.1157800_1157807delinsTTTTTTTC	NCBI36
NG_007460.2:g.22395_22402delinsTTTTTTTC , LRG_319:g.22395_22402delinsTTTTTTTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.-113_-106delinsTTTTTTTC	ENSP00000490268.2:n.-113_-106delinsTTTTTTTC
ENST00000585748.3:c.-82-11616_-82-11609delinsTTTTTTTC	ENSP00000477641.2:n.-82-11616_-82-11609delinsTTTTTTTC
ENST00000326873.12:c.-113_-106delinsTTTTTTTC MANE Select	ENSP00000324856.6:n.-113_-106delinsTTTTTTTC
ENST00000652231.1:c.-113_-106delinsTTTTTTTC	ENSP00000498804.1:n.-113_-106delinsTTTTTTTC
ENST00000326873.11:c.-113_-106delinsTTTTTTTC	ENSP00000324856.6:n.-113_-106delinsTTTTTTTC
ENST00000585748.2:c.-82-11616_-82-11609delinsTTTTTTTC	ENSP00000477641.1:n.-82-11616_-82-11609delinsTTTTTTTC
ENST00000586243.5:c.-113_-106delinsTTTTTTTC	ENSP00000467240.2:n.-113_-106delinsTTTTTTTC
NM_000455.4:c.-113_-106delinsTTTTTTTC , LRG_319t1:c.-113_-106delinsTTTTTTTC	NP_000446.1:n.-113_-106delinsTTTTTTTC
XM_005259617.1:c.-113_-106delinsTTTTTTTC	XP_005259674.1:n.-113_-106delinsTTTTTTTC
XM_005259618.3:c.-113_-106delinsTTTTTTTC	XP_005259675.1:n.-113_-106delinsTTTTTTTC
XM_011528209.1:c.-466_-459delinsTTTTTTTC	XP_011526511.1:n.-466_-459delinsTTTTTTTC
XR_936204.1:n.513_520delinsTTTTTTTC
XM_005259617.3:c.-113_-106delinsTTTTTTTC	XP_005259674.1:n.-113_-106delinsTTTTTTTC
XM_011528209.2:c.-466_-459delinsTTTTTTTC	XP_011526511.1:n.-466_-459delinsTTTTTTTC
XR_001753738.2:n.513_520delinsTTTTTTTC
XR_001753739.1:n.513_520delinsTTTTTTTC
XR_001753740.2:n.513_520delinsTTTTTTTC
NM_000455.5:c.-113_-106delinsTTTTTTTC MANE Select	NP_000446.1:n.-113_-106delinsTTTTTTTC