Canonical Allele Identifier: CA349714

Gene: STK11

Linked Data

• ClinVar Variation Id: 219507
• ClinVar RCV Id: RCV001824682 ; RCV002381701 ; RCV001448289
• dbSNP Id: rs864622128
• MyVariant Identifiers: chr19:g.1221209A>G (hg19) ; chr19:g.1221210A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1221210A>G , CM000681.2:g.1221210A>G	GRCh38
NC_000019.9:g.1221209A>G , CM000681.1:g.1221209A>G	GRCh37
NC_000019.8:g.1172209A>G	NCBI36
NG_007460.2:g.36804A>G , LRG_319:g.36804A>G

Transcript Alleles

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