Canonical Allele Identifier: CA631299516

Gene: STK11

Linked Data

• dbSNP Id: rs1568708559
• gnomAD v2: 19-1220765-G-GT
• gnomAD v3: 19-1220766-G-GT
• gnomAD v4: 19-1220766-G-GT
• MyVariant Identifiers: chr19:g.1220765_1220766insT (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1220766_1220767insT , CM000681.2:g.1220766_1220767insT	GRCh38
NC_000019.9:g.1220765_1220766insT , CM000681.1:g.1220765_1220766insT	GRCh37
NC_000019.8:g.1171765_1171766insT	NCBI36
NG_007460.2:g.36360_36361insT , LRG_319:g.36360_36361insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.734+49_734+50insT	ENSP00000490268.2:n.734+49_734+50insT
ENST00000585748.3:c.362+49_362+50insT	ENSP00000477641.2:n.362+49_362+50insT
ENST00000585851.2:c.560+49_560+50insT	ENSP00000467912.2:n.560+49_560+50insT
ENST00000326873.12:c.734+49_734+50insT MANE Select	ENSP00000324856.6:n.734+49_734+50insT
ENST00000652231.1:c.734+49_734+50insT	ENSP00000498804.1:n.734+49_734+50insT
ENST00000326873.11:c.734+49_734+50insT	ENSP00000324856.6:n.734+49_734+50insT
ENST00000586243.5:c.734+49_734+50insT	ENSP00000467240.2:n.734+49_734+50insT
ENST00000586358.5:n.632+49_632+50insT
ENST00000589152.5:n.824+49_824+50insT
ENST00000591133.2:n.705+49_705+50insT
NM_000455.4:c.734+49_734+50insT , LRG_319t1:c.734+49_734+50insT	NP_000446.1:n.734+49_734+50insT
XM_005259617.1:c.734+49_734+50insT	XP_005259674.1:n.734+49_734+50insT
XM_005259618.3:c.734+49_734+50insT	XP_005259675.1:n.734+49_734+50insT
XM_011528209.1:c.512+49_512+50insT	XP_011526511.1:n.512+49_512+50insT
XR_936204.1:n.1359+49_1359+50insT
XM_005259617.3:c.734+49_734+50insT	XP_005259674.1:n.734+49_734+50insT
XM_011528209.2:c.512+49_512+50insT	XP_011526511.1:n.512+49_512+50insT
XR_001753738.2:n.1359+49_1359+50insT
XR_001753739.1:n.1359+49_1359+50insT
XR_001753740.2:n.1359+49_1359+50insT
NM_000455.5:c.734+49_734+50insT MANE Select	NP_000446.1:n.734+49_734+50insT