Canonical Allele Identifier: CA3039112030
Gene: STK11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1218520_1218521insTGTGTTTG , CM000681.2:g.1218520_1218521insTGTGTTTG GRCh38
NC_000019.9:g.1218519_1218520insTGTGTTTG , CM000681.1:g.1218519_1218520insTGTGTTTG GRCh37
NC_000019.8:g.1169519_1169520insTGTGTTTG NCBI36
NG_007460.2:g.34114_34115insTGTGTTTG , LRG_319:g.34114_34115insTGTGTTTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000585465.3:c.374+20_374+21insTGTGTTTG ENSP00000490268.2:n.374+20_374+21insTGTGTTTG
ENST00000585748.3:c.2+20_2+21insTGTGTTTG ENSP00000477641.2:n.2+20_2+21insTGTGTTTG
ENST00000585851.2:c.291-1853_291-1852insTGTGTTTG ENSP00000467912.2:n.291-1853_291-1852insTGTGTTTG
ENST00000326873.12:c.374+20_374+21insTGTGTTTG MANE Select ENSP00000324856.6:n.374+20_374+21insTGTGTTTG
ENST00000652231.1:c.374+20_374+21insTGTGTTTG ENSP00000498804.1:n.374+20_374+21insTGTGTTTG
ENST00000326873.11:c.374+20_374+21insTGTGTTTG ENSP00000324856.6:n.374+20_374+21insTGTGTTTG
ENST00000585748.2:c.2+20_2+21insTGTGTTTG ENSP00000477641.1:n.2+20_2+21insTGTGTTTG
ENST00000585851.1:c.291-1853_291-1852insTGTGTTTG ENSP00000467912.1:n.291-1853_291-1852insTGTGTTTG
ENST00000586243.5:c.374+20_374+21insTGTGTTTG ENSP00000467240.2:n.374+20_374+21insTGTGTTTG
ENST00000586358.5:n.197+20_197+21insTGTGTTTG
ENST00000589152.5:n.464+20_464+21insTGTGTTTG
ENST00000593219.5:c.*199+20_*199+21insTGTGTTTG ENSP00000466610.1:n.*199+20_*199+21insTGTGTTTG
NM_000455.4:c.374+20_374+21insTGTGTTTG , LRG_319t1:c.374+20_374+21insTGTGTTTG NP_000446.1:n.374+20_374+21insTGTGTTTG
XM_005259617.1:c.374+20_374+21insTGTGTTTG XP_005259674.1:n.374+20_374+21insTGTGTTTG
XM_005259618.3:c.374+20_374+21insTGTGTTTG XP_005259675.1:n.374+20_374+21insTGTGTTTG
XM_011528209.1:c.152+20_152+21insTGTGTTTG XP_011526511.1:n.152+20_152+21insTGTGTTTG
XR_936204.1:n.999+20_999+21insTGTGTTTG
XM_005259617.3:c.374+20_374+21insTGTGTTTG XP_005259674.1:n.374+20_374+21insTGTGTTTG
XM_011528209.2:c.152+20_152+21insTGTGTTTG XP_011526511.1:n.152+20_152+21insTGTGTTTG
XR_001753738.2:n.999+20_999+21insTGTGTTTG
XR_001753739.1:n.999+20_999+21insTGTGTTTG
XR_001753740.2:n.999+20_999+21insTGTGTTTG
NM_000455.5:c.374+20_374+21insTGTGTTTG MANE Select NP_000446.1:n.374+20_374+21insTGTGTTTG