Canonical Allele Identifier: CA2317589251

Gene: STK11

Linked Data

• dbSNP Id: rs2080768000
• gnomAD v4: 19-1219552-G-GA

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1219552_1219553insA , CM000681.2:g.1219552_1219553insA	GRCh38
NC_000019.9:g.1219551_1219552insA , CM000681.1:g.1219551_1219552insA	GRCh37
NC_000019.8:g.1170551_1170552insA	NCBI36
NG_007460.2:g.35146_35147insA , LRG_319:g.35146_35147insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.464+139_464+140insA	ENSP00000490268.2:n.464+139_464+140insA
ENST00000585748.3:c.92+139_92+140insA	ENSP00000477641.2:n.92+139_92+140insA
ENST00000585851.2:c.291-821_291-820insA	ENSP00000467912.2:n.291-821_291-820insA
ENST00000326873.12:c.464+139_464+140insA MANE Select	ENSP00000324856.6:n.464+139_464+140insA
ENST00000652231.1:c.464+139_464+140insA	ENSP00000498804.1:n.464+139_464+140insA
ENST00000326873.11:c.464+139_464+140insA	ENSP00000324856.6:n.464+139_464+140insA
ENST00000585851.1:c.291-821_291-820insA	ENSP00000467912.1:n.291-821_291-820insA
ENST00000586243.5:c.464+139_464+140insA	ENSP00000467240.2:n.464+139_464+140insA
ENST00000586358.5:n.287+139_287+140insA
ENST00000589152.5:n.554+139_554+140insA
NM_000455.4:c.464+139_464+140insA , LRG_319t1:c.464+139_464+140insA	NP_000446.1:n.464+139_464+140insA
XM_005259617.1:c.464+139_464+140insA	XP_005259674.1:n.464+139_464+140insA
XM_005259618.3:c.464+139_464+140insA	XP_005259675.1:n.464+139_464+140insA
XM_011528209.1:c.242+139_242+140insA	XP_011526511.1:n.242+139_242+140insA
XR_936204.1:n.1089+139_1089+140insA
XM_005259617.3:c.464+139_464+140insA	XP_005259674.1:n.464+139_464+140insA
XM_011528209.2:c.242+139_242+140insA	XP_011526511.1:n.242+139_242+140insA
XR_001753738.2:n.1089+139_1089+140insA
XR_001753739.1:n.1089+139_1089+140insA
XR_001753740.2:n.1089+139_1089+140insA
NM_000455.5:c.464+139_464+140insA MANE Select	NP_000446.1:n.464+139_464+140insA