Canonical Allele Identifier: CA2317589315

Gene: STK11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1219650_1219653delinsATTC , CM000681.2:g.1219650_1219653delinsATTC	GRCh38
NC_000019.9:g.1219649_1219652delinsATTC , CM000681.1:g.1219649_1219652delinsATTC	GRCh37
NC_000019.8:g.1170649_1170652delinsATTC	NCBI36
NG_007460.2:g.35244_35247delinsATTC , LRG_319:g.35244_35247delinsATTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.464+237_464+240delinsATTC	ENSP00000490268.2:n.464+237_464+240delinsATTC
ENST00000585748.3:c.92+237_92+240delinsATTC	ENSP00000477641.2:n.92+237_92+240delinsATTC
ENST00000585851.2:c.291-723_291-720delinsATTC	ENSP00000467912.2:n.291-723_291-720delinsATTC
ENST00000326873.12:c.464+237_464+240delinsATTC MANE Select	ENSP00000324856.6:n.464+237_464+240delinsATTC
ENST00000652231.1:c.464+237_464+240delinsATTC	ENSP00000498804.1:n.464+237_464+240delinsATTC
ENST00000326873.11:c.464+237_464+240delinsATTC	ENSP00000324856.6:n.464+237_464+240delinsATTC
ENST00000585851.1:c.291-723_291-720delinsATTC	ENSP00000467912.1:n.291-723_291-720delinsATTC
ENST00000586243.5:c.464+237_464+240delinsATTC	ENSP00000467240.2:n.464+237_464+240delinsATTC
ENST00000586358.5:n.287+237_287+240delinsATTC
ENST00000589152.5:n.554+237_554+240delinsATTC
NM_000455.4:c.464+237_464+240delinsATTC , LRG_319t1:c.464+237_464+240delinsATTC	NP_000446.1:n.464+237_464+240delinsATTC
XM_005259617.1:c.464+237_464+240delinsATTC	XP_005259674.1:n.464+237_464+240delinsATTC
XM_005259618.3:c.464+237_464+240delinsATTC	XP_005259675.1:n.464+237_464+240delinsATTC
XM_011528209.1:c.242+237_242+240delinsATTC	XP_011526511.1:n.242+237_242+240delinsATTC
XR_936204.1:n.1089+237_1089+240delinsATTC
XM_005259617.3:c.464+237_464+240delinsATTC	XP_005259674.1:n.464+237_464+240delinsATTC
XM_011528209.2:c.242+237_242+240delinsATTC	XP_011526511.1:n.242+237_242+240delinsATTC
XR_001753738.2:n.1089+237_1089+240delinsATTC
XR_001753739.1:n.1089+237_1089+240delinsATTC
XR_001753740.2:n.1089+237_1089+240delinsATTC
NM_000455.5:c.464+237_464+240delinsATTC MANE Select	NP_000446.1:n.464+237_464+240delinsATTC