Canonical Allele Identifier: CA504707759

Gene: STK11

Linked Data

• ClinVar Variation Id: 717767
• ClinVar RCV Id: RCV001450211
• dbSNP Id: rs1599929398
• gnomAD v4: 19-1223057-G-A
• MyVariant Identifiers: chr19:g.1223056G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1223057G>A , CM000681.2:g.1223057G>A	GRCh38
NC_000019.9:g.1223056G>A , CM000681.1:g.1223056G>A	GRCh37
NC_000019.8:g.1174056G>A	NCBI36
NG_007460.2:g.38651G>A , LRG_319:g.38651G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.993G>A	ENSP00000490268.2:p.Arg331=
ENST00000585748.3:c.621G>A	ENSP00000477641.2:p.Arg207=
ENST00000585851.2:c.819G>A	ENSP00000467912.2:p.Arg273=
ENST00000326873.12:c.993G>A MANE Select	ENSP00000324856.6:p.Arg331=
ENST00000652231.1:c.993G>A	ENSP00000498804.1:p.Arg331=
ENST00000326873.11:c.993G>A	ENSP00000324856.6:p.Arg331=
ENST00000586243.5:c.993G>A	ENSP00000467240.2:p.Arg331=
ENST00000589152.5:n.1691G>A
ENST00000591133.2:n.964G>A
NM_000455.4:c.993G>A , LRG_319t1:c.993G>A	NP_000446.1:p.Arg331=
XM_005259617.1:c.993G>A	XP_005259674.1:p.Arg331=
XM_005259618.3:c.993G>A	XP_005259675.1:p.Arg331=
XM_011528209.1:c.771G>A	XP_011526511.1:p.Arg257=
XR_936204.1:n.1769G>A
XM_005259617.3:c.993G>A	XP_005259674.1:p.Arg331=
XM_011528209.2:c.771G>A	XP_011526511.1:p.Arg257=
XR_001753738.2:n.1799G>A
XR_001753739.1:n.1799G>A
XR_001753740.2:n.1769G>A
NM_000455.5:c.993G>A MANE Select	NP_000446.1:p.Arg331=