Canonical Allele Identifier: CA2317590074
Gene: STK11 HGNC NCBI

Linked Data

dbSNP Id: rs2080778577

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1220853_1220857dup , CM000681.2:g.1220853_1220857dup GRCh38
NC_000019.9:g.1220852_1220856dup , CM000681.1:g.1220852_1220856dup GRCh37
NC_000019.8:g.1171852_1171856dup NCBI36
NG_007460.2:g.36447_36451dup , LRG_319:g.36447_36451dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000585465.3:c.734+136_734+140dup ENSP00000490268.2:n.734+136_734+140dup
ENST00000585748.3:c.362+136_362+140dup ENSP00000477641.2:n.362+136_362+140dup
ENST00000585851.2:c.560+136_560+140dup ENSP00000467912.2:n.560+136_560+140dup
ENST00000326873.12:c.734+136_734+140dup MANE Select ENSP00000324856.6:n.734+136_734+140dup
ENST00000652231.1:c.734+136_734+140dup ENSP00000498804.1:n.734+136_734+140dup
ENST00000326873.11:c.734+136_734+140dup ENSP00000324856.6:n.734+136_734+140dup
ENST00000586243.5:c.734+136_734+140dup ENSP00000467240.2:n.734+136_734+140dup
ENST00000586358.5:n.632+136_632+140dup
ENST00000589152.5:n.824+136_824+140dup
ENST00000591133.2:n.705+136_705+140dup
NM_000455.4:c.734+136_734+140dup , LRG_319t1:c.734+136_734+140dup NP_000446.1:n.734+136_734+140dup
XM_005259617.1:c.734+136_734+140dup XP_005259674.1:n.734+136_734+140dup
XM_005259618.3:c.734+136_734+140dup XP_005259675.1:n.734+136_734+140dup
XM_011528209.1:c.512+136_512+140dup XP_011526511.1:n.512+136_512+140dup
XR_936204.1:n.1359+136_1359+140dup
XM_005259617.3:c.734+136_734+140dup XP_005259674.1:n.734+136_734+140dup
XM_011528209.2:c.512+136_512+140dup XP_011526511.1:n.512+136_512+140dup
XR_001753738.2:n.1359+136_1359+140dup
XR_001753739.1:n.1359+136_1359+140dup
XR_001753740.2:n.1359+136_1359+140dup
NM_000455.5:c.734+136_734+140dup MANE Select NP_000446.1:n.734+136_734+140dup