Canonical Allele Identifier: CA402954289

Gene: STK11

Linked Data

• dbSNP Id: rs1057523149
• gnomAD v4: 19-1226639-C-G
• MyVariant Identifiers: chr19:g.1226638C>G (hg19) ; chr19:g.1226639C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1226639C>G , CM000681.2:g.1226639C>G	GRCh38
NC_000019.9:g.1226638C>G , CM000681.1:g.1226638C>G	GRCh37
NC_000019.8:g.1177638C>G	NCBI36
NG_007460.2:g.42233C>G , LRG_319:g.42233C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.*2895C>G	ENSP00000490268.2:n.*2895C>G
ENST00000585748.3:c.922C>G	ENSP00000477641.2:p.Gln308Glu
ENST00000585851.2:c.1120C>G	ENSP00000467912.2:p.Gln374Glu
ENST00000326873.12:c.1294C>G MANE Select	ENSP00000324856.6:p.Gln432Glu
ENST00000326873.11:c.1294C>G	ENSP00000324856.6:p.Gln432Glu
ENST00000585465.2:n.3027C>G
ENST00000586243.5:c.1291C>G	ENSP00000467240.2:p.Gln431Glu
ENST00000589152.5:n.1992C>G
NM_000455.4:c.1294C>G , LRG_319t1:c.1294C>G	NP_000446.1:p.Gln432Glu
XM_005259617.1:c.1289C>G	XP_005259674.1:p.Ala430Gly
XM_011528209.1:c.1067C>G	XP_011526511.1:p.Ala356Gly
XM_005259617.3:c.1289C>G	XP_005259674.1:p.Ala430Gly
XM_011528209.2:c.1067C>G	XP_011526511.1:p.Ala356Gly
XR_001753738.2:n.2100C>G
XR_001753740.2:n.2070C>G
NM_000455.5:c.1294C>G MANE Select	NP_000446.1:p.Gln432Glu