Canonical Allele Identifier: CA2317593778

Gene: STK11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1226606_1226608delinsAGC , CM000681.2:g.1226606_1226608delinsAGC	GRCh38
NC_000019.9:g.1226605_1226607delinsAGC , CM000681.1:g.1226605_1226607delinsAGC	GRCh37
NC_000019.8:g.1177605_1177607delinsAGC	NCBI36
NG_007460.2:g.42200_42202delinsAGC , LRG_319:g.42200_42202delinsAGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.*2862_*2864delinsAGC	ENSP00000490268.2:n.*2862_*2864delinsAGC
ENST00000585748.3:c.889_891delinsAGC	ENSP00000477641.2:p.Ser297=
ENST00000585851.2:c.1087_1089delinsAGC	ENSP00000467912.2:p.Ser363=
ENST00000326873.12:c.1261_1263delinsAGC MANE Select	ENSP00000324856.6:p.Ser421=
ENST00000326873.11:c.1261_1263delinsAGC	ENSP00000324856.6:p.Ser421=
ENST00000585465.2:n.2994_2996delinsAGC
ENST00000586243.5:c.1258_1260delinsAGC	ENSP00000467240.2:p.Ser420=
ENST00000589152.5:n.1959_1961delinsAGC
NM_000455.4:c.1261_1263delinsAGC , LRG_319t1:c.1261_1263delinsAGC	NP_000446.1:p.Ser421=
XM_005259617.1:c.1256_1258delinsAGC	XP_005259674.1:p.Gln419=
XM_011528209.1:c.1034_1036delinsAGC	XP_011526511.1:p.Gln345=
XM_005259617.3:c.1256_1258delinsAGC	XP_005259674.1:p.Gln419=
XM_011528209.2:c.1034_1036delinsAGC	XP_011526511.1:p.Gln345=
XR_001753738.2:n.2067_2069delinsAGC
XR_001753740.2:n.2037_2039delinsAGC
NM_000455.5:c.1261_1263delinsAGC MANE Select	NP_000446.1:p.Ser421=