Canonical Allele Identifier: CA2317581683

Gene: STK11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1207111_1207112delinsGC , CM000681.2:g.1207111_1207112delinsGC	GRCh38
NC_000019.9:g.1207110_1207111delinsGC , CM000681.1:g.1207110_1207111delinsGC	GRCh37
NC_000019.8:g.1158110_1158111delinsGC	NCBI36
NG_007460.2:g.22705_22706delinsGC , LRG_319:g.22705_22706delinsGC

Transcript Alleles

HGVS	Amino-acid change
ENST00000585465.3:c.198_199delinsGC	ENSP00000490268.2:p.Val66=
ENST00000585748.3:c.-82-11306_-82-11305delinsGC	ENSP00000477641.2:n.-82-11306_-82-11305delinsGC
ENST00000585851.2:c.198_199delinsGC	ENSP00000467912.2:p.Val66=
ENST00000326873.12:c.198_199delinsGC MANE Select	ENSP00000324856.6:p.Val66=
ENST00000652231.1:c.198_199delinsGC	ENSP00000498804.1:p.Val66=
ENST00000326873.11:c.198_199delinsGC	ENSP00000324856.6:p.Val66=
ENST00000585748.2:c.-82-11306_-82-11305delinsGC	ENSP00000477641.1:n.-82-11306_-82-11305delinsGC
ENST00000585851.1:c.198_199delinsGC	ENSP00000467912.1:p.Val66=
ENST00000586243.5:c.198_199delinsGC	ENSP00000467240.2:p.Val66=
ENST00000586358.5:n.21_22delinsGC
ENST00000589152.5:n.288_289delinsGC
ENST00000593219.5:c.198_199delinsGC	ENSP00000466610.1:p.Val66=
NM_000455.4:c.198_199delinsGC , LRG_319t1:c.198_199delinsGC	NP_000446.1:p.Val66=
XM_005259617.1:c.198_199delinsGC	XP_005259674.1:p.Val66=
XM_005259618.3:c.198_199delinsGC	XP_005259675.1:p.Val66=
XM_011528209.1:c.-156_-155delinsGC	XP_011526511.1:n.-156_-155delinsGC
XR_936204.1:n.823_824delinsGC
XM_005259617.3:c.198_199delinsGC	XP_005259674.1:p.Val66=
XM_011528209.2:c.-156_-155delinsGC	XP_011526511.1:n.-156_-155delinsGC
XR_001753738.2:n.823_824delinsGC
XR_001753739.1:n.823_824delinsGC
XR_001753740.2:n.823_824delinsGC
NM_000455.5:c.198_199delinsGC MANE Select	NP_000446.1:p.Val66=