Canonical Allele Identifier: CA2317581440

Gene: STK11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1206796_1206801delinsCCTTTT , CM000681.2:g.1206796_1206801delinsCCTTTT	GRCh38
NC_000019.9:g.1206795_1206800delinsCCTTTT , CM000681.1:g.1206795_1206800delinsCCTTTT	GRCh37
NC_000019.8:g.1157795_1157800delinsCCTTTT	NCBI36
NG_007460.2:g.22390_22395delinsCCTTTT , LRG_319:g.22390_22395delinsCCTTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.-118_-113delinsCCTTTT	ENSP00000490268.2:n.-118_-113delinsCCTTTT
ENST00000585748.3:c.-82-11621_-82-11616delinsCCTTTT	ENSP00000477641.2:n.-82-11621_-82-11616delinsCCTTTT
ENST00000326873.12:c.-118_-113delinsCCTTTT MANE Select	ENSP00000324856.6:n.-118_-113delinsCCTTTT
ENST00000652231.1:c.-118_-113delinsCCTTTT	ENSP00000498804.1:n.-118_-113delinsCCTTTT
ENST00000326873.11:c.-118_-113delinsCCTTTT	ENSP00000324856.6:n.-118_-113delinsCCTTTT
ENST00000585748.2:c.-82-11621_-82-11616delinsCCTTTT	ENSP00000477641.1:n.-82-11621_-82-11616delinsCCTTTT
ENST00000586243.5:c.-118_-113delinsCCTTTT	ENSP00000467240.2:n.-118_-113delinsCCTTTT
NM_000455.4:c.-118_-113delinsCCTTTT , LRG_319t1:c.-118_-113delinsCCTTTT	NP_000446.1:n.-118_-113delinsCCTTTT
XM_005259617.1:c.-118_-113delinsCCTTTT	XP_005259674.1:n.-118_-113delinsCCTTTT
XM_005259618.3:c.-118_-113delinsCCTTTT	XP_005259675.1:n.-118_-113delinsCCTTTT
XM_011528209.1:c.-471_-466delinsCCTTTT	XP_011526511.1:n.-471_-466delinsCCTTTT
XR_936204.1:n.508_513delinsCCTTTT
XM_005259617.3:c.-118_-113delinsCCTTTT	XP_005259674.1:n.-118_-113delinsCCTTTT
XM_011528209.2:c.-471_-466delinsCCTTTT	XP_011526511.1:n.-471_-466delinsCCTTTT
XR_001753738.2:n.508_513delinsCCTTTT
XR_001753739.1:n.508_513delinsCCTTTT
XR_001753740.2:n.508_513delinsCCTTTT
NM_000455.5:c.-118_-113delinsCCTTTT MANE Select	NP_000446.1:n.-118_-113delinsCCTTTT