Canonical Allele Identifier: CA2582592119

Gene: STK11

Linked Data

• gnomAD v4: 19-1219441-G-GTGGC

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1219441_1219442insTGGC , CM000681.2:g.1219441_1219442insTGGC	GRCh38
NC_000019.9:g.1219440_1219441insTGGC , CM000681.1:g.1219440_1219441insTGGC	GRCh37
NC_000019.8:g.1170440_1170441insTGGC	NCBI36
NG_007460.2:g.35035_35036insTGGC , LRG_319:g.35035_35036insTGGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.464+28_464+29insTGGC	ENSP00000490268.2:n.464+28_464+29insTGGC
ENST00000585748.3:c.92+28_92+29insTGGC	ENSP00000477641.2:n.92+28_92+29insTGGC
ENST00000585851.2:c.291-932_291-931insTGGC	ENSP00000467912.2:n.291-932_291-931insTGGC
ENST00000326873.12:c.464+28_464+29insTGGC MANE Select	ENSP00000324856.6:n.464+28_464+29insTGGC
ENST00000652231.1:c.464+28_464+29insTGGC	ENSP00000498804.1:n.464+28_464+29insTGGC
ENST00000326873.11:c.464+28_464+29insTGGC	ENSP00000324856.6:n.464+28_464+29insTGGC
ENST00000585851.1:c.291-932_291-931insTGGC	ENSP00000467912.1:n.291-932_291-931insTGGC
ENST00000586243.5:c.464+28_464+29insTGGC	ENSP00000467240.2:n.464+28_464+29insTGGC
ENST00000586358.5:n.287+28_287+29insTGGC
ENST00000589152.5:n.554+28_554+29insTGGC
NM_000455.4:c.464+28_464+29insTGGC , LRG_319t1:c.464+28_464+29insTGGC	NP_000446.1:n.464+28_464+29insTGGC
XM_005259617.1:c.464+28_464+29insTGGC	XP_005259674.1:n.464+28_464+29insTGGC
XM_005259618.3:c.464+28_464+29insTGGC	XP_005259675.1:n.464+28_464+29insTGGC
XM_011528209.1:c.242+28_242+29insTGGC	XP_011526511.1:n.242+28_242+29insTGGC
XR_936204.1:n.1089+28_1089+29insTGGC
XM_005259617.3:c.464+28_464+29insTGGC	XP_005259674.1:n.464+28_464+29insTGGC
XM_011528209.2:c.242+28_242+29insTGGC	XP_011526511.1:n.242+28_242+29insTGGC
XR_001753738.2:n.1089+28_1089+29insTGGC
XR_001753739.1:n.1089+28_1089+29insTGGC
XR_001753740.2:n.1089+28_1089+29insTGGC
NM_000455.5:c.464+28_464+29insTGGC MANE Select	NP_000446.1:n.464+28_464+29insTGGC