Canonical Allele Identifier: CA2582590994

Gene: STK11

Linked Data

• gnomAD v4: 19-1206682-G-GCCCGCCGGTCCGCAGAC

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1206685_1206701dup , CM000681.2:g.1206685_1206701dup	GRCh38
NC_000019.9:g.1206684_1206700dup , CM000681.1:g.1206684_1206700dup	GRCh37
NC_000019.8:g.1157684_1157700dup	NCBI36
NG_007460.2:g.22279_22295dup , LRG_319:g.22279_22295dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.-229_-213dup	ENSP00000490268.2:n.-229_-213dup
ENST00000585748.3:c.-82-11732_-82-11716dup	ENSP00000477641.2:n.-82-11732_-82-11716dup
ENST00000326873.12:c.-229_-213dup MANE Select	ENSP00000324856.6:n.-229_-213dup
ENST00000652231.1:c.-229_-213dup	ENSP00000498804.1:n.-229_-213dup
ENST00000326873.11:c.-229_-213dup	ENSP00000324856.6:n.-229_-213dup
ENST00000585748.2:c.-82-11732_-82-11716dup	ENSP00000477641.1:n.-82-11732_-82-11716dup
ENST00000586243.5:c.-229_-213dup	ENSP00000467240.2:n.-229_-213dup
NM_000455.4:c.-229_-213dup , LRG_319t1:c.-229_-213dup	NP_000446.1:n.-229_-213dup
XM_005259617.1:c.-229_-213dup	XP_005259674.1:n.-229_-213dup
XM_005259618.3:c.-229_-213dup	XP_005259675.1:n.-229_-213dup
XM_011528209.1:c.-582_-566dup	XP_011526511.1:n.-582_-566dup
XR_936204.1:n.397_413dup
XM_005259617.3:c.-229_-213dup	XP_005259674.1:n.-229_-213dup
XM_011528209.2:c.-582_-566dup	XP_011526511.1:n.-582_-566dup
XR_001753738.2:n.397_413dup
XR_001753739.1:n.397_413dup
XR_001753740.2:n.397_413dup
NM_000455.5:c.-229_-213dup MANE Select	NP_000446.1:n.-229_-213dup