Canonical Allele Identifier: CA2317590114
Gene: STK11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1220932_1220934delinsTCA , CM000681.2:g.1220932_1220934delinsTCA GRCh38
NC_000019.9:g.1220931_1220933delinsTCA , CM000681.1:g.1220931_1220933delinsTCA GRCh37
NC_000019.8:g.1171931_1171933delinsTCA NCBI36
NG_007460.2:g.36526_36528delinsTCA , LRG_319:g.36526_36528delinsTCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000585465.3:c.734+215_734+217delinsTCA ENSP00000490268.2:n.734+215_734+217delinsTCA
ENST00000585748.3:c.362+215_362+217delinsTCA ENSP00000477641.2:n.362+215_362+217delinsTCA
ENST00000585851.2:c.560+215_560+217delinsTCA ENSP00000467912.2:n.560+215_560+217delinsTCA
ENST00000326873.12:c.734+215_734+217delinsTCA MANE Select ENSP00000324856.6:n.734+215_734+217delinsTCA
ENST00000652231.1:c.734+215_734+217delinsTCA ENSP00000498804.1:n.734+215_734+217delinsTCA
ENST00000326873.11:c.734+215_734+217delinsTCA ENSP00000324856.6:n.734+215_734+217delinsTCA
ENST00000586243.5:c.734+215_734+217delinsTCA ENSP00000467240.2:n.734+215_734+217delinsTCA
ENST00000586358.5:n.632+215_632+217delinsTCA
ENST00000589152.5:n.824+215_824+217delinsTCA
ENST00000591133.2:n.705+215_705+217delinsTCA
NM_000455.4:c.734+215_734+217delinsTCA , LRG_319t1:c.734+215_734+217delinsTCA NP_000446.1:n.734+215_734+217delinsTCA
XM_005259617.1:c.734+215_734+217delinsTCA XP_005259674.1:n.734+215_734+217delinsTCA
XM_005259618.3:c.734+215_734+217delinsTCA XP_005259675.1:n.734+215_734+217delinsTCA
XM_011528209.1:c.512+215_512+217delinsTCA XP_011526511.1:n.512+215_512+217delinsTCA
XR_936204.1:n.1359+215_1359+217delinsTCA
XM_005259617.3:c.734+215_734+217delinsTCA XP_005259674.1:n.734+215_734+217delinsTCA
XM_011528209.2:c.512+215_512+217delinsTCA XP_011526511.1:n.512+215_512+217delinsTCA
XR_001753738.2:n.1359+215_1359+217delinsTCA
XR_001753739.1:n.1359+215_1359+217delinsTCA
XR_001753740.2:n.1359+215_1359+217delinsTCA
NM_000455.5:c.734+215_734+217delinsTCA MANE Select NP_000446.1:n.734+215_734+217delinsTCA