Canonical Allele Identifier: CA2582591577

Gene: STK11

Linked Data

• gnomAD v4: 19-1207352-G-GGCT

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1207353_1207354insCTG , CM000681.2:g.1207353_1207354insCTG	GRCh38
NC_000019.9:g.1207352_1207353insCTG , CM000681.1:g.1207352_1207353insCTG	GRCh37
NC_000019.8:g.1158352_1158353insCTG	NCBI36
NG_007460.2:g.22947_22948insCTG , LRG_319:g.22947_22948insCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.290+150_290+151insCTG	ENSP00000490268.2:n.290+150_290+151insCTG
ENST00000585748.3:c.-82-11064_-82-11063insCTG	ENSP00000477641.2:n.-82-11064_-82-11063insCTG
ENST00000585851.2:c.290+150_290+151insCTG	ENSP00000467912.2:n.290+150_290+151insCTG
ENST00000326873.12:c.290+150_290+151insCTG MANE Select	ENSP00000324856.6:n.290+150_290+151insCTG
ENST00000652231.1:c.290+150_290+151insCTG	ENSP00000498804.1:n.290+150_290+151insCTG
ENST00000326873.11:c.290+150_290+151insCTG	ENSP00000324856.6:n.290+150_290+151insCTG
ENST00000585748.2:c.-82-11064_-82-11063insCTG	ENSP00000477641.1:n.-82-11064_-82-11063insCTG
ENST00000585851.1:c.290+150_290+151insCTG	ENSP00000467912.1:n.290+150_290+151insCTG
ENST00000586243.5:c.290+150_290+151insCTG	ENSP00000467240.2:n.290+150_290+151insCTG
ENST00000586358.5:n.113+150_113+151insCTG
ENST00000589152.5:n.380+150_380+151insCTG
ENST00000593219.5:c.290+150_290+151insCTG	ENSP00000466610.1:n.290+150_290+151insCTG
NM_000455.4:c.290+150_290+151insCTG , LRG_319t1:c.290+150_290+151insCTG	NP_000446.1:n.290+150_290+151insCTG
XM_005259617.1:c.290+150_290+151insCTG	XP_005259674.1:n.290+150_290+151insCTG
XM_005259618.3:c.290+150_290+151insCTG	XP_005259675.1:n.290+150_290+151insCTG
XM_011528209.1:c.-64+150_-64+151insCTG	XP_011526511.1:n.-64+150_-64+151insCTG
XR_936204.1:n.915+150_915+151insCTG
XM_005259617.3:c.290+150_290+151insCTG	XP_005259674.1:n.290+150_290+151insCTG
XM_011528209.2:c.-64+150_-64+151insCTG	XP_011526511.1:n.-64+150_-64+151insCTG
XR_001753738.2:n.915+150_915+151insCTG
XR_001753739.1:n.915+150_915+151insCTG
XR_001753740.2:n.915+150_915+151insCTG
NM_000455.5:c.290+150_290+151insCTG MANE Select	NP_000446.1:n.290+150_290+151insCTG