Canonical Allele Identifier: CA2966064358

Gene: STK11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1218418dup , CM000681.2:g.1218418dup	GRCh38
NC_000019.9:g.1218417dup , CM000681.1:g.1218417dup	GRCh37
NC_000019.8:g.1169417dup	NCBI36
NG_007460.2:g.34012dup , LRG_319:g.34012dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.292dup
ENST00000585748.3:c.-81dup
ENST00000585851.2:c.291-1955dup	ENSP00000467912.2:n.291-1955dup
ENST00000326873.12:c.292dup
ENST00000652231.1:c.292dup
ENST00000326873.11:c.292dup
ENST00000585748.2:c.-81dup
ENST00000585851.1:c.291-1955dup	ENSP00000467912.1:n.291-1955dup
ENST00000586243.5:c.292dup
ENST00000586358.5:n.115dup
ENST00000589152.5:n.382dup
ENST00000593219.5:c.*117dup
NM_000455.4:c.292dup , LRG_319t1:c.292dup
XM_005259617.1:c.292dup
XM_005259618.3:c.292dup
XM_011528209.1:c.70dup
XR_936204.1:n.917dup
XM_005259617.3:c.292dup
XM_011528209.2:c.70dup
XR_001753738.2:n.917dup
XR_001753739.1:n.917dup
XR_001753740.2:n.917dup
NM_000455.5:c.292dup