Canonical Allele Identifier: CA645604082

Gene: STK11

Linked Data

• COSMIC: COSM49012

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1220568_1220589del , CM000681.2:g.1220568_1220589del	GRCh38
NC_000019.9:g.1220567_1220588del , CM000681.1:g.1220567_1220588del	GRCh37
NC_000019.8:g.1171567_1171588del	NCBI36
NG_007460.2:g.36162_36183del , LRG_319:g.36162_36183del

Transcript Alleles

HGVS	Amino-acid change
ENST00000585465.3:c.598-13_606del
ENST00000585748.3:c.226-13_234del
ENST00000585851.2:c.424-13_432del
ENST00000326873.12:c.598-13_606del
ENST00000652231.1:c.598-13_606del
ENST00000326873.11:c.598-13_606del
ENST00000585851.1:c.424-13_432del
ENST00000586243.5:c.598-13_606del
ENST00000586358.5:n.483_504del
ENST00000589152.5:n.688-13_696del
ENST00000591133.2:n.556_577del
NM_000455.4:c.598-13_606del , LRG_319t1:c.598-13_606del
XM_005259617.1:c.598-13_606del
XM_005259618.3:c.598-13_606del
XM_011528209.1:c.376-13_384del
XR_936204.1:n.1223-13_1231del
XM_005259617.3:c.598-13_606del
XM_011528209.2:c.376-13_384del
XR_001753738.2:n.1223-13_1231del
XR_001753739.1:n.1223-13_1231del
XR_001753740.2:n.1223-13_1231del
NM_000455.5:c.598-13_606del