Canonical Allele Identifier: CA2582597100

Gene: STK11

Linked Data

• gnomAD v4: 19-1226334-GGGGCGGGCATGGCCT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1226339_1226353del , CM000681.2:g.1226339_1226353del	GRCh38
NC_000019.9:g.1226338_1226352del , CM000681.1:g.1226338_1226352del	GRCh37
NC_000019.8:g.1177338_1177352del	NCBI36
NG_007460.2:g.41933_41947del , LRG_319:g.41933_41947del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.*2595_*2609del	ENSP00000490268.2:n.*2595_*2609del
ENST00000585748.3:c.737-115_737-101del	ENSP00000477641.2:n.737-115_737-101del
ENST00000585851.2:c.935-115_935-101del	ENSP00000467912.2:n.935-115_935-101del
ENST00000326873.12:c.1109-115_1109-101del MANE Select	ENSP00000324856.6:n.1109-115_1109-101del
ENST00000326873.11:c.1109-115_1109-101del	ENSP00000324856.6:n.1109-115_1109-101del
ENST00000585465.2:n.2727_2741del
ENST00000586243.5:c.1109-115_1109-101del	ENSP00000467240.2:n.1109-115_1109-101del
ENST00000589152.5:n.1807-115_1807-101del
NM_000455.4:c.1109-115_1109-101del , LRG_319t1:c.1109-115_1109-101del	NP_000446.1:n.1109-115_1109-101del
XM_005259617.1:c.1109-120_1109-106del	XP_005259674.1:n.1109-120_1109-106del
XM_011528209.1:c.887-120_887-106del	XP_011526511.1:n.887-120_887-106del
XM_005259617.3:c.1109-120_1109-106del	XP_005259674.1:n.1109-120_1109-106del
XM_011528209.2:c.887-120_887-106del	XP_011526511.1:n.887-120_887-106del
XR_001753738.2:n.1915-115_1915-101del
XR_001753740.2:n.1885-115_1885-101del
NM_000455.5:c.1109-115_1109-101del MANE Select	NP_000446.1:n.1109-115_1109-101del