Canonical Allele Identifier: CA2317588435

Gene: STK11

Linked Data

• dbSNP Id: rs2080757305

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1218271_1218286del , CM000681.2:g.1218271_1218286del	GRCh38
NC_000019.9:g.1218270_1218285del , CM000681.1:g.1218270_1218285del	GRCh37
NC_000019.8:g.1169270_1169285del	NCBI36
NG_007460.2:g.33865_33880del , LRG_319:g.33865_33880del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.291-146_291-131del	ENSP00000490268.2:n.291-146_291-131del
ENST00000585748.3:c.-82-146_-82-131del	ENSP00000477641.2:n.-82-146_-82-131del
ENST00000585851.2:c.291-2102_291-2087del	ENSP00000467912.2:n.291-2102_291-2087del
ENST00000326873.12:c.291-146_291-131del MANE Select	ENSP00000324856.6:n.291-146_291-131del
ENST00000652231.1:c.291-146_291-131del	ENSP00000498804.1:n.291-146_291-131del
ENST00000326873.11:c.291-146_291-131del	ENSP00000324856.6:n.291-146_291-131del
ENST00000585748.2:c.-82-146_-82-131del	ENSP00000477641.1:n.-82-146_-82-131del
ENST00000585851.1:c.291-2102_291-2087del	ENSP00000467912.1:n.291-2102_291-2087del
ENST00000586243.5:c.291-146_291-131del	ENSP00000467240.2:n.291-146_291-131del
ENST00000586358.5:n.114-146_114-131del
ENST00000589152.5:n.381-146_381-131del
ENST00000593219.5:c.*116-146_*116-131del	ENSP00000466610.1:n.*116-146_*116-131del
NM_000455.4:c.291-146_291-131del , LRG_319t1:c.291-146_291-131del	NP_000446.1:n.291-146_291-131del
XM_005259617.1:c.291-146_291-131del	XP_005259674.1:n.291-146_291-131del
XM_005259618.3:c.291-146_291-131del	XP_005259675.1:n.291-146_291-131del
XM_011528209.1:c.69-146_69-131del	XP_011526511.1:n.69-146_69-131del
XR_936204.1:n.916-146_916-131del
XM_005259617.3:c.291-146_291-131del	XP_005259674.1:n.291-146_291-131del
XM_011528209.2:c.69-146_69-131del	XP_011526511.1:n.69-146_69-131del
XR_001753738.2:n.916-146_916-131del
XR_001753739.1:n.916-146_916-131del
XR_001753740.2:n.916-146_916-131del
NM_000455.5:c.291-146_291-131del MANE Select	NP_000446.1:n.291-146_291-131del