Canonical Allele Identifier: CA402954194

Gene: STK11

Linked Data

• dbSNP Id: rs1222940657
• MyVariant Identifiers: chr19:g.1226623C>G (hg19) ; chr19:g.1226624C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1226624C>G , CM000681.2:g.1226624C>G	GRCh38
NC_000019.9:g.1226623C>G , CM000681.1:g.1226623C>G	GRCh37
NC_000019.8:g.1177623C>G	NCBI36
NG_007460.2:g.42218C>G , LRG_319:g.42218C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.*2880C>G	ENSP00000490268.2:n.*2880C>G
ENST00000585748.3:c.907C>G	ENSP00000477641.2:p.Leu303Val
ENST00000585851.2:c.1105C>G	ENSP00000467912.2:p.Leu369Val
ENST00000326873.12:c.1279C>G MANE Select	ENSP00000324856.6:p.Leu427Val
ENST00000326873.11:c.1279C>G	ENSP00000324856.6:p.Leu427Val
ENST00000585465.2:n.3012C>G
ENST00000586243.5:c.1276C>G	ENSP00000467240.2:p.Leu426Val
ENST00000589152.5:n.1977C>G
NM_000455.4:c.1279C>G , LRG_319t1:c.1279C>G	NP_000446.1:p.Leu427Val
XM_005259617.1:c.1274C>G	XP_005259674.1:p.Ala425Gly
XM_011528209.1:c.1052C>G	XP_011526511.1:p.Ala351Gly
XM_005259617.3:c.1274C>G	XP_005259674.1:p.Ala425Gly
XM_011528209.2:c.1052C>G	XP_011526511.1:p.Ala351Gly
XR_001753738.2:n.2085C>G
XR_001753740.2:n.2055C>G
NM_000455.5:c.1279C>G MANE Select	NP_000446.1:p.Leu427Val