Canonical Allele Identifier: CA2317589245

Gene: STK11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1219546_1219554delinsTTTTTTGTG , CM000681.2:g.1219546_1219554delinsTTTTTTGTG	GRCh38
NC_000019.9:g.1219545_1219553delinsTTTTTTGTG , CM000681.1:g.1219545_1219553delinsTTTTTTGTG	GRCh37
NC_000019.8:g.1170545_1170553delinsTTTTTTGTG	NCBI36
NG_007460.2:g.35140_35148delinsTTTTTTGTG , LRG_319:g.35140_35148delinsTTTTTTGTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.464+133_464+141delinsTTTTTTGTG	ENSP00000490268.2:n.464+133_464+141delinsTTTTTTGTG
ENST00000585748.3:c.92+133_92+141delinsTTTTTTGTG	ENSP00000477641.2:n.92+133_92+141delinsTTTTTTGTG
ENST00000585851.2:c.291-827_291-819delinsTTTTTTGTG	ENSP00000467912.2:n.291-827_291-819delinsTTTTTTGTG
ENST00000326873.12:c.464+133_464+141delinsTTTTTTGTG MANE Select	ENSP00000324856.6:n.464+133_464+141delinsTTTTTTGTG
ENST00000652231.1:c.464+133_464+141delinsTTTTTTGTG	ENSP00000498804.1:n.464+133_464+141delinsTTTTTTGTG
ENST00000326873.11:c.464+133_464+141delinsTTTTTTGTG	ENSP00000324856.6:n.464+133_464+141delinsTTTTTTGTG
ENST00000585851.1:c.291-827_291-819delinsTTTTTTGTG	ENSP00000467912.1:n.291-827_291-819delinsTTTTTTGTG
ENST00000586243.5:c.464+133_464+141delinsTTTTTTGTG	ENSP00000467240.2:n.464+133_464+141delinsTTTTTTGTG
ENST00000586358.5:n.287+133_287+141delinsTTTTTTGTG
ENST00000589152.5:n.554+133_554+141delinsTTTTTTGTG
NM_000455.4:c.464+133_464+141delinsTTTTTTGTG , LRG_319t1:c.464+133_464+141delinsTTTTTTGTG	NP_000446.1:n.464+133_464+141delinsTTTTTTGTG
XM_005259617.1:c.464+133_464+141delinsTTTTTTGTG	XP_005259674.1:n.464+133_464+141delinsTTTTTTGTG
XM_005259618.3:c.464+133_464+141delinsTTTTTTGTG	XP_005259675.1:n.464+133_464+141delinsTTTTTTGTG
XM_011528209.1:c.242+133_242+141delinsTTTTTTGTG	XP_011526511.1:n.242+133_242+141delinsTTTTTTGTG
XR_936204.1:n.1089+133_1089+141delinsTTTTTTGTG
XM_005259617.3:c.464+133_464+141delinsTTTTTTGTG	XP_005259674.1:n.464+133_464+141delinsTTTTTTGTG
XM_011528209.2:c.242+133_242+141delinsTTTTTTGTG	XP_011526511.1:n.242+133_242+141delinsTTTTTTGTG
XR_001753738.2:n.1089+133_1089+141delinsTTTTTTGTG
XR_001753739.1:n.1089+133_1089+141delinsTTTTTTGTG
XR_001753740.2:n.1089+133_1089+141delinsTTTTTTGTG
NM_000455.5:c.464+133_464+141delinsTTTTTTGTG MANE Select	NP_000446.1:n.464+133_464+141delinsTTTTTTGTG