Canonical Allele Identifier: CA2317581556

Gene: STK11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1206944_1206947delinsATGT , CM000681.2:g.1206944_1206947delinsATGT	GRCh38
NC_000019.9:g.1206943_1206946delinsATGT , CM000681.1:g.1206943_1206946delinsATGT	GRCh37
NC_000019.8:g.1157943_1157946delinsATGT	NCBI36
NG_007460.2:g.22538_22541delinsATGT , LRG_319:g.22538_22541delinsATGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.31_34delinsATGT	ENSP00000490268.2:p.Met11=
ENST00000585748.3:c.-82-11473_-82-11470delinsATGT	ENSP00000477641.2:n.-82-11473_-82-11470delinsATGT
ENST00000585851.2:c.31_34delinsATGT	ENSP00000467912.2:p.Met11=
ENST00000326873.12:c.31_34delinsATGT MANE Select	ENSP00000324856.6:p.Met11=
ENST00000652231.1:c.31_34delinsATGT	ENSP00000498804.1:p.Met11=
ENST00000326873.11:c.31_34delinsATGT	ENSP00000324856.6:p.Met11=
ENST00000585748.2:c.-82-11473_-82-11470delinsATGT	ENSP00000477641.1:n.-82-11473_-82-11470delinsATGT
ENST00000585851.1:c.31_34delinsATGT	ENSP00000467912.1:p.Met11=
ENST00000586243.5:c.31_34delinsATGT	ENSP00000467240.2:p.Met11=
ENST00000589152.5:n.121_124delinsATGT
ENST00000593219.5:c.31_34delinsATGT	ENSP00000466610.1:p.Met11=
NM_000455.4:c.31_34delinsATGT , LRG_319t1:c.31_34delinsATGT	NP_000446.1:p.Met11=
XM_005259617.1:c.31_34delinsATGT	XP_005259674.1:p.Met11=
XM_005259618.3:c.31_34delinsATGT	XP_005259675.1:p.Met11=
XM_011528209.1:c.-323_-320delinsATGT	XP_011526511.1:n.-323_-320delinsATGT
XR_936204.1:n.656_659delinsATGT
XM_005259617.3:c.31_34delinsATGT	XP_005259674.1:p.Met11=
XM_011528209.2:c.-323_-320delinsATGT	XP_011526511.1:n.-323_-320delinsATGT
XR_001753738.2:n.656_659delinsATGT
XR_001753739.1:n.656_659delinsATGT
XR_001753740.2:n.656_659delinsATGT
NM_000455.5:c.31_34delinsATGT MANE Select	NP_000446.1:p.Met11=