Canonical Allele Identifier: CA631299719

Gene: STK11

Linked Data

• dbSNP Id: rs1305155905
• gnomAD v2: 19-1206868-G-GC
• gnomAD v4: 19-1206869-G-GC
• MyVariant Identifiers: chr19:g.1206868_1206869insC (hg19) ; chr19:g.1206869_1206870insC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1206870dup , CM000681.2:g.1206870dup	GRCh38
NC_000019.9:g.1206869dup , CM000681.1:g.1206869dup	GRCh37
NC_000019.8:g.1157869dup	NCBI36
NG_007460.2:g.22464dup , LRG_319:g.22464dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.-44dup	ENSP00000490268.2:n.-44dup
ENST00000585748.3:c.-82-11547dup	ENSP00000477641.2:n.-82-11547dup
ENST00000585851.2:c.-44dup	ENSP00000467912.2:n.-44dup
ENST00000326873.12:c.-44dup MANE Select	ENSP00000324856.6:n.-44dup
ENST00000652231.1:c.-44dup	ENSP00000498804.1:n.-44dup
ENST00000326873.11:c.-44dup	ENSP00000324856.6:n.-44dup
ENST00000585748.2:c.-82-11547dup	ENSP00000477641.1:n.-82-11547dup
ENST00000585851.1:c.-44dup	ENSP00000467912.1:n.-44dup
ENST00000586243.5:c.-44dup	ENSP00000467240.2:n.-44dup
ENST00000589152.5:n.47dup
ENST00000593219.5:c.-44dup	ENSP00000466610.1:n.-44dup
NM_000455.4:c.-44dup , LRG_319t1:c.-44dup	NP_000446.1:n.-44dup
XM_005259617.1:c.-44dup	XP_005259674.1:n.-44dup
XM_005259618.3:c.-44dup	XP_005259675.1:n.-44dup
XM_011528209.1:c.-397dup	XP_011526511.1:n.-397dup
XR_936204.1:n.582dup
XM_005259617.3:c.-44dup	XP_005259674.1:n.-44dup
XM_011528209.2:c.-397dup	XP_011526511.1:n.-397dup
XR_001753738.2:n.582dup
XR_001753739.1:n.582dup
XR_001753740.2:n.582dup
NM_000455.5:c.-44dup MANE Select	NP_000446.1:n.-44dup