Canonical Allele Identifier: CA2813238242

Gene: STK11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1219548_1219551del , CM000681.2:g.1219548_1219551del	GRCh38
NC_000019.9:g.1219547_1219550del , CM000681.1:g.1219547_1219550del	GRCh37
NC_000019.8:g.1170547_1170550del	NCBI36
NG_007460.2:g.35142_35145del , LRG_319:g.35142_35145del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.464+135_464+138del	ENSP00000490268.2:n.464+135_464+138del
ENST00000585748.3:c.92+135_92+138del	ENSP00000477641.2:n.92+135_92+138del
ENST00000585851.2:c.291-825_291-822del	ENSP00000467912.2:n.291-825_291-822del
ENST00000326873.12:c.464+135_464+138del MANE Select	ENSP00000324856.6:n.464+135_464+138del
ENST00000652231.1:c.464+135_464+138del	ENSP00000498804.1:n.464+135_464+138del
ENST00000326873.11:c.464+135_464+138del	ENSP00000324856.6:n.464+135_464+138del
ENST00000585851.1:c.291-825_291-822del	ENSP00000467912.1:n.291-825_291-822del
ENST00000586243.5:c.464+135_464+138del	ENSP00000467240.2:n.464+135_464+138del
ENST00000586358.5:n.287+135_287+138del
ENST00000589152.5:n.554+135_554+138del
NM_000455.4:c.464+135_464+138del , LRG_319t1:c.464+135_464+138del	NP_000446.1:n.464+135_464+138del
XM_005259617.1:c.464+135_464+138del	XP_005259674.1:n.464+135_464+138del
XM_005259618.3:c.464+135_464+138del	XP_005259675.1:n.464+135_464+138del
XM_011528209.1:c.242+135_242+138del	XP_011526511.1:n.242+135_242+138del
XR_936204.1:n.1089+135_1089+138del
XM_005259617.3:c.464+135_464+138del	XP_005259674.1:n.464+135_464+138del
XM_011528209.2:c.242+135_242+138del	XP_011526511.1:n.242+135_242+138del
XR_001753738.2:n.1089+135_1089+138del
XR_001753739.1:n.1089+135_1089+138del
XR_001753740.2:n.1089+135_1089+138del
NM_000455.5:c.464+135_464+138del MANE Select	NP_000446.1:n.464+135_464+138del