Canonical Allele Identifier: CA304024009

Gene: STK11

Linked Data

• dbSNP Id: rs56814888
• gnomAD v2: 19-1218143-G-GAA
• gnomAD v3: 19-1218144-G-GAA
• gnomAD v4: 19-1218144-G-GAA
• MyVariant Identifiers: chr19:g.1218144_1218145insAA (hg19) ; chr19:g.1218145_1218146insAA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1218155_1218156dup , CM000681.2:g.1218155_1218156dup	GRCh38
NC_000019.9:g.1218154_1218155dup , CM000681.1:g.1218154_1218155dup	GRCh37
NC_000019.8:g.1169154_1169155dup	NCBI36
NG_007460.2:g.33749_33750dup , LRG_319:g.33749_33750dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.291-262_291-261dup	ENSP00000490268.2:n.291-262_291-261dup
ENST00000585748.3:c.-82-262_-82-261dup	ENSP00000477641.2:n.-82-262_-82-261dup
ENST00000585851.2:c.291-2218_291-2217dup	ENSP00000467912.2:n.291-2218_291-2217dup
ENST00000326873.12:c.291-262_291-261dup MANE Select	ENSP00000324856.6:n.291-262_291-261dup
ENST00000652231.1:c.291-262_291-261dup	ENSP00000498804.1:n.291-262_291-261dup
ENST00000326873.11:c.291-262_291-261dup	ENSP00000324856.6:n.291-262_291-261dup
ENST00000585748.2:c.-82-262_-82-261dup	ENSP00000477641.1:n.-82-262_-82-261dup
ENST00000585851.1:c.291-2218_291-2217dup	ENSP00000467912.1:n.291-2218_291-2217dup
ENST00000586243.5:c.291-262_291-261dup	ENSP00000467240.2:n.291-262_291-261dup
ENST00000586358.5:n.114-262_114-261dup
ENST00000589152.5:n.381-262_381-261dup
ENST00000593219.5:c.*116-262_*116-261dup	ENSP00000466610.1:n.*116-262_*116-261dup
NM_000455.4:c.291-262_291-261dup , LRG_319t1:c.291-262_291-261dup	NP_000446.1:n.291-262_291-261dup
XM_005259617.1:c.291-262_291-261dup	XP_005259674.1:n.291-262_291-261dup
XM_005259618.3:c.291-262_291-261dup	XP_005259675.1:n.291-262_291-261dup
XM_011528209.1:c.69-262_69-261dup	XP_011526511.1:n.69-262_69-261dup
XR_936204.1:n.916-262_916-261dup
XM_005259617.3:c.291-262_291-261dup	XP_005259674.1:n.291-262_291-261dup
XM_011528209.2:c.69-262_69-261dup	XP_011526511.1:n.69-262_69-261dup
XR_001753738.2:n.916-262_916-261dup
XR_001753739.1:n.916-262_916-261dup
XR_001753740.2:n.916-262_916-261dup
NM_000455.5:c.291-262_291-261dup MANE Select	NP_000446.1:n.291-262_291-261dup