Canonical Allele Identifier: CA402954068

Gene: STK11

Linked Data

• MyVariant Identifiers: chr19:g.1226603C>G (hg19) ; chr19:g.1226604C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1226604C>G , CM000681.2:g.1226604C>G	GRCh38
NC_000019.9:g.1226603C>G , CM000681.1:g.1226603C>G	GRCh37
NC_000019.8:g.1177603C>G	NCBI36
NG_007460.2:g.42198C>G , LRG_319:g.42198C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.*2860C>G	ENSP00000490268.2:n.*2860C>G
ENST00000585748.3:c.887C>G	ENSP00000477641.2:p.Ala296Gly
ENST00000585851.2:c.1085C>G	ENSP00000467912.2:p.Ala362Gly
ENST00000326873.12:c.1259C>G MANE Select	ENSP00000324856.6:p.Ala420Gly
ENST00000326873.11:c.1259C>G	ENSP00000324856.6:p.Ala420Gly
ENST00000585465.2:n.2992C>G
ENST00000586243.5:c.1256C>G	ENSP00000467240.2:p.Ala419Gly
ENST00000589152.5:n.1957C>G
NM_000455.4:c.1259C>G , LRG_319t1:c.1259C>G	NP_000446.1:p.Ala420Gly
XM_005259617.1:c.1254C>G	XP_005259674.1:p.Arg418=
XM_011528209.1:c.1032C>G	XP_011526511.1:p.Arg344=
XM_005259617.3:c.1254C>G	XP_005259674.1:p.Arg418=
XM_011528209.2:c.1032C>G	XP_011526511.1:p.Arg344=
XR_001753738.2:n.2065C>G
XR_001753740.2:n.2035C>G
NM_000455.5:c.1259C>G MANE Select	NP_000446.1:p.Ala420Gly