Canonical Allele Identifier: CA2317593780

Gene: STK11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1226607_1226608delinsGC , CM000681.2:g.1226607_1226608delinsGC	GRCh38
NC_000019.9:g.1226606_1226607delinsGC , CM000681.1:g.1226606_1226607delinsGC	GRCh37
NC_000019.8:g.1177606_1177607delinsGC	NCBI36
NG_007460.2:g.42201_42202delinsGC , LRG_319:g.42201_42202delinsGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.*2863_*2864delinsGC	ENSP00000490268.2:n.*2863_*2864delinsGC
ENST00000585748.3:c.890_891delinsGC	ENSP00000477641.2:p.Ser297=
ENST00000585851.2:c.1088_1089delinsGC	ENSP00000467912.2:p.Ser363=
ENST00000326873.12:c.1262_1263delinsGC MANE Select	ENSP00000324856.6:p.Ser421=
ENST00000326873.11:c.1262_1263delinsGC	ENSP00000324856.6:p.Ser421=
ENST00000585465.2:n.2995_2996delinsGC
ENST00000586243.5:c.1259_1260delinsGC	ENSP00000467240.2:p.Ser420=
ENST00000589152.5:n.1960_1961delinsGC
NM_000455.4:c.1262_1263delinsGC , LRG_319t1:c.1262_1263delinsGC	NP_000446.1:p.Ser421=
XM_005259617.1:c.1257_1258delinsGC	XP_005259674.1:p.Gln419=
XM_011528209.1:c.1035_1036delinsGC	XP_011526511.1:p.Gln345=
XM_005259617.3:c.1257_1258delinsGC	XP_005259674.1:p.Gln419=
XM_011528209.2:c.1035_1036delinsGC	XP_011526511.1:p.Gln345=
XR_001753738.2:n.2068_2069delinsGC
XR_001753740.2:n.2038_2039delinsGC
NM_000455.5:c.1262_1263delinsGC MANE Select	NP_000446.1:p.Ser421=