Canonical Allele Identifier: CA645604081

Gene: STK11

Linked Data

• COSMIC: COSM1731602

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1220530_1220544del , CM000681.2:g.1220530_1220544del	GRCh38
NC_000019.9:g.1220529_1220543del , CM000681.1:g.1220529_1220543del	GRCh37
NC_000019.8:g.1171529_1171543del	NCBI36
NG_007460.2:g.36124_36138del , LRG_319:g.36124_36138del

Transcript Alleles

HGVS	Amino-acid change
ENST00000585465.3:c.597+25_598-37del	ENSP00000490268.2:n.597+25_598-37del
ENST00000585748.3:c.225+25_226-37del	ENSP00000477641.2:n.225+25_226-37del
ENST00000585851.2:c.423+25_424-37del	ENSP00000467912.2:n.423+25_424-37del
ENST00000326873.12:c.597+25_598-37del MANE Select	ENSP00000324856.6:n.597+25_598-37del
ENST00000652231.1:c.597+25_598-37del	ENSP00000498804.1:n.597+25_598-37del
ENST00000326873.11:c.597+25_598-37del	ENSP00000324856.6:n.597+25_598-37del
ENST00000585851.1:c.423+25_424-37del	ENSP00000467912.1:n.423+25_424-37del
ENST00000586243.5:c.597+25_598-37del	ENSP00000467240.2:n.597+25_598-37del
ENST00000586358.5:n.445_459del
ENST00000589152.5:n.687+25_688-37del
ENST00000591133.2:n.518_532del
NM_000455.4:c.597+25_598-37del , LRG_319t1:c.597+25_598-37del	NP_000446.1:n.597+25_598-37del
XM_005259617.1:c.597+25_598-37del	XP_005259674.1:n.597+25_598-37del
XM_005259618.3:c.597+25_598-37del	XP_005259675.1:n.597+25_598-37del
XM_011528209.1:c.375+25_376-37del	XP_011526511.1:n.375+25_376-37del
XR_936204.1:n.1222+25_1223-37del
XM_005259617.3:c.597+25_598-37del	XP_005259674.1:n.597+25_598-37del
XM_011528209.2:c.375+25_376-37del	XP_011526511.1:n.375+25_376-37del
XR_001753738.2:n.1222+25_1223-37del
XR_001753739.1:n.1222+25_1223-37del
XR_001753740.2:n.1222+25_1223-37del
NM_000455.5:c.597+25_598-37del MANE Select	NP_000446.1:n.597+25_598-37del