Canonical Allele Identifier: CA046170

Gene: STK11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1226605_1226608del , CM000681.2:g.1226605_1226608del	GRCh38
NC_000019.9:g.1226604_1226607del , CM000681.1:g.1226604_1226607del	GRCh37
NC_000019.8:g.1177604_1177607del	NCBI36
NG_007460.2:g.42199_42202del , LRG_319:g.42199_42202del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.*2861_*2864del	ENSP00000490268.2:n.*2861_*2864del
ENST00000585748.3:c.888_891del	ENSP00000477641.2:p.Ser297AlafsTer?
ENST00000585851.2:c.1086_1089del	ENSP00000467912.2:p.Ser363AlafsTer?
ENST00000326873.12:c.1260_1263del MANE Select	ENSP00000324856.6:p.Ser421AlafsTer?
ENST00000326873.11:c.1260_1263del	ENSP00000324856.6:p.Ser421AlafsTer?
ENST00000585465.2:n.2993_2996del
ENST00000586243.5:c.1257_1260del	ENSP00000467240.2:p.Ser420AlafsTer?
ENST00000589152.5:n.1958_1961del
NM_000455.4:c.1260_1263del , LRG_319t1:c.1260_1263del	NP_000446.1:p.Ser421AlafsTer?
XM_005259617.1:c.1255_1258del	XP_005259674.1:p.Gln419SerfsTer13
XM_011528209.1:c.1033_1036del	XP_011526511.1:p.Gln345SerfsTer13
XM_005259617.3:c.1255_1258del	XP_005259674.1:p.Gln419SerfsTer13
XM_011528209.2:c.1033_1036del	XP_011526511.1:p.Gln345SerfsTer13
XR_001753738.2:n.2066_2069del
XR_001753740.2:n.2036_2039del
NM_000455.5:c.1260_1263del MANE Select	NP_000446.1:p.Ser421AlafsTer?