Canonical Allele Identifier: CA2582592121

Gene: STK11

Linked Data

• gnomAD v4: 19-1219442-G-GAGC

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1219442_1219443insAGC , CM000681.2:g.1219442_1219443insAGC	GRCh38
NC_000019.9:g.1219441_1219442insAGC , CM000681.1:g.1219441_1219442insAGC	GRCh37
NC_000019.8:g.1170441_1170442insAGC	NCBI36
NG_007460.2:g.35036_35037insAGC , LRG_319:g.35036_35037insAGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.464+29_464+30insAGC	ENSP00000490268.2:n.464+29_464+30insAGC
ENST00000585748.3:c.92+29_92+30insAGC	ENSP00000477641.2:n.92+29_92+30insAGC
ENST00000585851.2:c.291-931_291-930insAGC	ENSP00000467912.2:n.291-931_291-930insAGC
ENST00000326873.12:c.464+29_464+30insAGC MANE Select	ENSP00000324856.6:n.464+29_464+30insAGC
ENST00000652231.1:c.464+29_464+30insAGC	ENSP00000498804.1:n.464+29_464+30insAGC
ENST00000326873.11:c.464+29_464+30insAGC	ENSP00000324856.6:n.464+29_464+30insAGC
ENST00000585851.1:c.291-931_291-930insAGC	ENSP00000467912.1:n.291-931_291-930insAGC
ENST00000586243.5:c.464+29_464+30insAGC	ENSP00000467240.2:n.464+29_464+30insAGC
ENST00000586358.5:n.287+29_287+30insAGC
ENST00000589152.5:n.554+29_554+30insAGC
NM_000455.4:c.464+29_464+30insAGC , LRG_319t1:c.464+29_464+30insAGC	NP_000446.1:n.464+29_464+30insAGC
XM_005259617.1:c.464+29_464+30insAGC	XP_005259674.1:n.464+29_464+30insAGC
XM_005259618.3:c.464+29_464+30insAGC	XP_005259675.1:n.464+29_464+30insAGC
XM_011528209.1:c.242+29_242+30insAGC	XP_011526511.1:n.242+29_242+30insAGC
XR_936204.1:n.1089+29_1089+30insAGC
XM_005259617.3:c.464+29_464+30insAGC	XP_005259674.1:n.464+29_464+30insAGC
XM_011528209.2:c.242+29_242+30insAGC	XP_011526511.1:n.242+29_242+30insAGC
XR_001753738.2:n.1089+29_1089+30insAGC
XR_001753739.1:n.1089+29_1089+30insAGC
XR_001753740.2:n.1089+29_1089+30insAGC
NM_000455.5:c.464+29_464+30insAGC MANE Select	NP_000446.1:n.464+29_464+30insAGC