Canonical Allele Identifier: CA2582592259

Gene: STK11

Linked Data

• gnomAD v4: 19-1219547-TTTTTGTG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1219552_1219558del , CM000681.2:g.1219552_1219558del	GRCh38
NC_000019.9:g.1219551_1219557del , CM000681.1:g.1219551_1219557del	GRCh37
NC_000019.8:g.1170551_1170557del	NCBI36
NG_007460.2:g.35146_35152del , LRG_319:g.35146_35152del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.464+139_464+145del	ENSP00000490268.2:n.464+139_464+145del
ENST00000585748.3:c.92+139_92+145del	ENSP00000477641.2:n.92+139_92+145del
ENST00000585851.2:c.291-821_291-815del	ENSP00000467912.2:n.291-821_291-815del
ENST00000326873.12:c.464+139_464+145del MANE Select	ENSP00000324856.6:n.464+139_464+145del
ENST00000652231.1:c.464+139_464+145del	ENSP00000498804.1:n.464+139_464+145del
ENST00000326873.11:c.464+139_464+145del	ENSP00000324856.6:n.464+139_464+145del
ENST00000585851.1:c.291-821_291-815del	ENSP00000467912.1:n.291-821_291-815del
ENST00000586243.5:c.464+139_464+145del	ENSP00000467240.2:n.464+139_464+145del
ENST00000586358.5:n.287+139_287+145del
ENST00000589152.5:n.554+139_554+145del
NM_000455.4:c.464+139_464+145del , LRG_319t1:c.464+139_464+145del	NP_000446.1:n.464+139_464+145del
XM_005259617.1:c.464+139_464+145del	XP_005259674.1:n.464+139_464+145del
XM_005259618.3:c.464+139_464+145del	XP_005259675.1:n.464+139_464+145del
XM_011528209.1:c.242+139_242+145del	XP_011526511.1:n.242+139_242+145del
XR_936204.1:n.1089+139_1089+145del
XM_005259617.3:c.464+139_464+145del	XP_005259674.1:n.464+139_464+145del
XM_011528209.2:c.242+139_242+145del	XP_011526511.1:n.242+139_242+145del
XR_001753738.2:n.1089+139_1089+145del
XR_001753739.1:n.1089+139_1089+145del
XR_001753740.2:n.1089+139_1089+145del
NM_000455.5:c.464+139_464+145del MANE Select	NP_000446.1:n.464+139_464+145del