Canonical Allele Identifier: CA304026517

Gene: STK11

Linked Data

• dbSNP Id: rs950031893
• gnomAD v3: 19-1220972-A-AG
• gnomAD v4: 19-1220972-A-AG
• MyVariant Identifiers: chr19:g.1220971_1220972insG (hg19) ; chr19:g.1220972_1220973insG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1220975dup , CM000681.2:g.1220975dup	GRCh38
NC_000019.9:g.1220974dup , CM000681.1:g.1220974dup	GRCh37
NC_000019.8:g.1171974dup	NCBI36
NG_007460.2:g.36569dup , LRG_319:g.36569dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.735-238dup	ENSP00000490268.2:n.735-238dup
ENST00000585748.3:c.363-238dup	ENSP00000477641.2:n.363-238dup
ENST00000585851.2:c.561-238dup	ENSP00000467912.2:n.561-238dup
ENST00000326873.12:c.735-238dup MANE Select	ENSP00000324856.6:n.735-238dup
ENST00000652231.1:c.735-238dup	ENSP00000498804.1:n.735-238dup
ENST00000326873.11:c.735-238dup	ENSP00000324856.6:n.735-238dup
ENST00000586243.5:c.735-238dup	ENSP00000467240.2:n.735-238dup
ENST00000586358.5:n.633-238dup
ENST00000589152.5:n.825-238dup
ENST00000591133.2:n.706-238dup
NM_000455.4:c.735-238dup , LRG_319t1:c.735-238dup	NP_000446.1:n.735-238dup
XM_005259617.1:c.735-238dup	XP_005259674.1:n.735-238dup
XM_005259618.3:c.735-238dup	XP_005259675.1:n.735-238dup
XM_011528209.1:c.513-238dup	XP_011526511.1:n.513-238dup
XR_936204.1:n.1360-238dup
XM_005259617.3:c.735-238dup	XP_005259674.1:n.735-238dup
XM_011528209.2:c.513-238dup	XP_011526511.1:n.513-238dup
XR_001753738.2:n.1360-238dup
XR_001753739.1:n.1360-238dup
XR_001753740.2:n.1360-238dup
NM_000455.5:c.735-238dup MANE Select	NP_000446.1:n.735-238dup