Canonical Allele Identifier: CA2966064483

Gene: STK11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1218506dup , CM000681.2:g.1218506dup	GRCh38
NC_000019.9:g.1218505dup , CM000681.1:g.1218505dup	GRCh37
NC_000019.8:g.1169505dup	NCBI36
NG_007460.2:g.34100dup , LRG_319:g.34100dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.374+6dup	ENSP00000490268.2:n.374+6dup
ENST00000585748.3:c.2+6dup	ENSP00000477641.2:n.2+6dup
ENST00000585851.2:c.291-1867dup	ENSP00000467912.2:n.291-1867dup
ENST00000326873.12:c.374+6dup MANE Select	ENSP00000324856.6:n.374+6dup
ENST00000652231.1:c.374+6dup	ENSP00000498804.1:n.374+6dup
ENST00000326873.11:c.374+6dup	ENSP00000324856.6:n.374+6dup
ENST00000585748.2:c.2+6dup	ENSP00000477641.1:n.2+6dup
ENST00000585851.1:c.291-1867dup	ENSP00000467912.1:n.291-1867dup
ENST00000586243.5:c.374+6dup	ENSP00000467240.2:n.374+6dup
ENST00000586358.5:n.197+6dup
ENST00000589152.5:n.464+6dup
ENST00000593219.5:c.*199+6dup	ENSP00000466610.1:n.*199+6dup
NM_000455.4:c.374+6dup , LRG_319t1:c.374+6dup	NP_000446.1:n.374+6dup
XM_005259617.1:c.374+6dup	XP_005259674.1:n.374+6dup
XM_005259618.3:c.374+6dup	XP_005259675.1:n.374+6dup
XM_011528209.1:c.152+6dup	XP_011526511.1:n.152+6dup
XR_936204.1:n.999+6dup
XM_005259617.3:c.374+6dup	XP_005259674.1:n.374+6dup
XM_011528209.2:c.152+6dup	XP_011526511.1:n.152+6dup
XR_001753738.2:n.999+6dup
XR_001753739.1:n.999+6dup
XR_001753740.2:n.999+6dup
NM_000455.5:c.374+6dup MANE Select	NP_000446.1:n.374+6dup