Canonical Allele Identifier: CA2582592117

Gene: STK11

Linked Data

• gnomAD v4: 19-1219440-T-TAGGGC

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1219440_1219441insAGGGC , CM000681.2:g.1219440_1219441insAGGGC	GRCh38
NC_000019.9:g.1219439_1219440insAGGGC , CM000681.1:g.1219439_1219440insAGGGC	GRCh37
NC_000019.8:g.1170439_1170440insAGGGC	NCBI36
NG_007460.2:g.35034_35035insAGGGC , LRG_319:g.35034_35035insAGGGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.464+27_464+28insAGGGC	ENSP00000490268.2:n.464+27_464+28insAGGGC
ENST00000585748.3:c.92+27_92+28insAGGGC	ENSP00000477641.2:n.92+27_92+28insAGGGC
ENST00000585851.2:c.291-933_291-932insAGGGC	ENSP00000467912.2:n.291-933_291-932insAGGGC
ENST00000326873.12:c.464+27_464+28insAGGGC MANE Select	ENSP00000324856.6:n.464+27_464+28insAGGGC
ENST00000652231.1:c.464+27_464+28insAGGGC	ENSP00000498804.1:n.464+27_464+28insAGGGC
ENST00000326873.11:c.464+27_464+28insAGGGC	ENSP00000324856.6:n.464+27_464+28insAGGGC
ENST00000585851.1:c.291-933_291-932insAGGGC	ENSP00000467912.1:n.291-933_291-932insAGGGC
ENST00000586243.5:c.464+27_464+28insAGGGC	ENSP00000467240.2:n.464+27_464+28insAGGGC
ENST00000586358.5:n.287+27_287+28insAGGGC
ENST00000589152.5:n.554+27_554+28insAGGGC
NM_000455.4:c.464+27_464+28insAGGGC , LRG_319t1:c.464+27_464+28insAGGGC	NP_000446.1:n.464+27_464+28insAGGGC
XM_005259617.1:c.464+27_464+28insAGGGC	XP_005259674.1:n.464+27_464+28insAGGGC
XM_005259618.3:c.464+27_464+28insAGGGC	XP_005259675.1:n.464+27_464+28insAGGGC
XM_011528209.1:c.242+27_242+28insAGGGC	XP_011526511.1:n.242+27_242+28insAGGGC
XR_936204.1:n.1089+27_1089+28insAGGGC
XM_005259617.3:c.464+27_464+28insAGGGC	XP_005259674.1:n.464+27_464+28insAGGGC
XM_011528209.2:c.242+27_242+28insAGGGC	XP_011526511.1:n.242+27_242+28insAGGGC
XR_001753738.2:n.1089+27_1089+28insAGGGC
XR_001753739.1:n.1089+27_1089+28insAGGGC
XR_001753740.2:n.1089+27_1089+28insAGGGC
NM_000455.5:c.464+27_464+28insAGGGC MANE Select	NP_000446.1:n.464+27_464+28insAGGGC