Canonical Allele Identifier: CA402954174

Gene: STK11

Linked Data

• dbSNP Id: rs2145436544
• MyVariant Identifiers: chr19:g.1226616C>G (hg19) ; chr19:g.1226617C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1226617C>G , CM000681.2:g.1226617C>G	GRCh38
NC_000019.9:g.1226616C>G , CM000681.1:g.1226616C>G	GRCh37
NC_000019.8:g.1177616C>G	NCBI36
NG_007460.2:g.42211C>G , LRG_319:g.42211C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.*2873C>G	ENSP00000490268.2:n.*2873C>G
ENST00000585748.3:c.900C>G	ENSP00000477641.2:p.Ile300Met
ENST00000585851.2:c.1098C>G	ENSP00000467912.2:p.Ile366Met
ENST00000326873.12:c.1272C>G MANE Select	ENSP00000324856.6:p.Ile424Met
ENST00000326873.11:c.1272C>G	ENSP00000324856.6:p.Ile424Met
ENST00000585465.2:n.3005C>G
ENST00000586243.5:c.1269C>G	ENSP00000467240.2:p.Ile423Met
ENST00000589152.5:n.1970C>G
NM_000455.4:c.1272C>G , LRG_319t1:c.1272C>G	NP_000446.1:p.Ile424Met
XM_005259617.1:c.1267C>G	XP_005259674.1:p.Pro423Ala
XM_011528209.1:c.1045C>G	XP_011526511.1:p.Pro349Ala
XM_005259617.3:c.1267C>G	XP_005259674.1:p.Pro423Ala
XM_011528209.2:c.1045C>G	XP_011526511.1:p.Pro349Ala
XR_001753738.2:n.2078C>G
XR_001753740.2:n.2048C>G
NM_000455.5:c.1272C>G MANE Select	NP_000446.1:p.Ile424Met