Canonical Allele Identifier: CA304016676

Gene: STK11

Linked Data

• dbSNP Id: rs869200084
• MyVariant Identifiers: chr19:g.1206896del (hg19) ; chr19:g.1206897del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1206897del , CM000681.2:g.1206897del	GRCh38
NC_000019.9:g.1206896del , CM000681.1:g.1206896del	GRCh37
NC_000019.8:g.1157896del	NCBI36
NG_007460.2:g.22491del , LRG_319:g.22491del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.-17del	ENSP00000490268.2:n.-17del
ENST00000585748.3:c.-82-11520del	ENSP00000477641.2:n.-82-11520del
ENST00000585851.2:c.-17del	ENSP00000467912.2:n.-17del
ENST00000326873.12:c.-17del MANE Select	ENSP00000324856.6:n.-17del
ENST00000652231.1:c.-17del	ENSP00000498804.1:n.-17del
ENST00000326873.11:c.-17del	ENSP00000324856.6:n.-17del
ENST00000585748.2:c.-82-11520del	ENSP00000477641.1:n.-82-11520del
ENST00000585851.1:c.-17del	ENSP00000467912.1:n.-17del
ENST00000586243.5:c.-17del	ENSP00000467240.2:n.-17del
ENST00000589152.5:n.74del
ENST00000593219.5:c.-17del	ENSP00000466610.1:n.-17del
NM_000455.4:c.-17del , LRG_319t1:c.-17del	NP_000446.1:n.-17del
XM_005259617.1:c.-17del	XP_005259674.1:n.-17del
XM_005259618.3:c.-17del	XP_005259675.1:n.-17del
XM_011528209.1:c.-370del	XP_011526511.1:n.-370del
XR_936204.1:n.609del
XM_005259617.3:c.-17del	XP_005259674.1:n.-17del
XM_011528209.2:c.-370del	XP_011526511.1:n.-370del
XR_001753738.2:n.609del
XR_001753739.1:n.609del
XR_001753740.2:n.609del
NM_000455.5:c.-17del MANE Select	NP_000446.1:n.-17del