Canonical Allele Identifier: CA2317593539

Gene: STK11

Linked Data

• dbSNP Id: rs2080819987

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1226290del , CM000681.2:g.1226290del	GRCh38
NC_000019.9:g.1226289del , CM000681.1:g.1226289del	GRCh37
NC_000019.8:g.1177289del	NCBI36
NG_007460.2:g.41884del , LRG_319:g.41884del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.*2546del	ENSP00000490268.2:n.*2546del
ENST00000585748.3:c.737-164del	ENSP00000477641.2:n.737-164del
ENST00000585851.2:c.935-164del	ENSP00000467912.2:n.935-164del
ENST00000326873.12:c.1109-164del MANE Select	ENSP00000324856.6:n.1109-164del
ENST00000326873.11:c.1109-164del	ENSP00000324856.6:n.1109-164del
ENST00000585465.2:n.2678del
ENST00000586243.5:c.1109-164del	ENSP00000467240.2:n.1109-164del
ENST00000589152.5:n.1807-164del
NM_000455.4:c.1109-164del , LRG_319t1:c.1109-164del	NP_000446.1:n.1109-164del
XM_005259617.1:c.1109-169del	XP_005259674.1:n.1109-169del
XM_011528209.1:c.887-169del	XP_011526511.1:n.887-169del
XM_005259617.3:c.1109-169del	XP_005259674.1:n.1109-169del
XM_011528209.2:c.887-169del	XP_011526511.1:n.887-169del
XR_001753738.2:n.1915-164del
XR_001753740.2:n.1885-164del
NM_000455.5:c.1109-164del MANE Select	NP_000446.1:n.1109-164del