Canonical Allele Identifier: CA2317589188

Gene: STK11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1219464_1219465delinsAG , CM000681.2:g.1219464_1219465delinsAG	GRCh38
NC_000019.9:g.1219463_1219464delinsAG , CM000681.1:g.1219463_1219464delinsAG	GRCh37
NC_000019.8:g.1170463_1170464delinsAG	NCBI36
NG_007460.2:g.35058_35059delinsAG , LRG_319:g.35058_35059delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.464+51_464+52delinsAG	ENSP00000490268.2:n.464+51_464+52delinsAG
ENST00000585748.3:c.92+51_92+52delinsAG	ENSP00000477641.2:n.92+51_92+52delinsAG
ENST00000585851.2:c.291-909_291-908delinsAG	ENSP00000467912.2:n.291-909_291-908delinsAG
ENST00000326873.12:c.464+51_464+52delinsAG MANE Select	ENSP00000324856.6:n.464+51_464+52delinsAG
ENST00000652231.1:c.464+51_464+52delinsAG	ENSP00000498804.1:n.464+51_464+52delinsAG
ENST00000326873.11:c.464+51_464+52delinsAG	ENSP00000324856.6:n.464+51_464+52delinsAG
ENST00000585851.1:c.291-909_291-908delinsAG	ENSP00000467912.1:n.291-909_291-908delinsAG
ENST00000586243.5:c.464+51_464+52delinsAG	ENSP00000467240.2:n.464+51_464+52delinsAG
ENST00000586358.5:n.287+51_287+52delinsAG
ENST00000589152.5:n.554+51_554+52delinsAG
NM_000455.4:c.464+51_464+52delinsAG , LRG_319t1:c.464+51_464+52delinsAG	NP_000446.1:n.464+51_464+52delinsAG
XM_005259617.1:c.464+51_464+52delinsAG	XP_005259674.1:n.464+51_464+52delinsAG
XM_005259618.3:c.464+51_464+52delinsAG	XP_005259675.1:n.464+51_464+52delinsAG
XM_011528209.1:c.242+51_242+52delinsAG	XP_011526511.1:n.242+51_242+52delinsAG
XR_936204.1:n.1089+51_1089+52delinsAG
XM_005259617.3:c.464+51_464+52delinsAG	XP_005259674.1:n.464+51_464+52delinsAG
XM_011528209.2:c.242+51_242+52delinsAG	XP_011526511.1:n.242+51_242+52delinsAG
XR_001753738.2:n.1089+51_1089+52delinsAG
XR_001753739.1:n.1089+51_1089+52delinsAG
XR_001753740.2:n.1089+51_1089+52delinsAG
NM_000455.5:c.464+51_464+52delinsAG MANE Select	NP_000446.1:n.464+51_464+52delinsAG