Canonical Allele Identifier: CA089242

Gene: STK11

Linked Data

• ClinVar Variation Id: 458014
• ClinVar RCV Id: RCV001798875
• dbSNP Id: rs1060499954
• gnomAD v4: 19-1207025-C-G
• MyVariant Identifiers: chr19:g.1207024C>G (hg19) ; chr19:g.1207025C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1207025C>G , CM000681.2:g.1207025C>G	GRCh38
NC_000019.9:g.1207024C>G , CM000681.1:g.1207024C>G	GRCh37
NC_000019.8:g.1158024C>G	NCBI36
NG_007460.2:g.22619C>G , LRG_319:g.22619C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000585465.3:c.112C>G	ENSP00000490268.2:p.Pro38Ala
ENST00000585748.3:c.-82-11392C>G	ENSP00000477641.2:n.-82-11392C>G
ENST00000585851.2:c.112C>G	ENSP00000467912.2:p.Pro38Ala
ENST00000326873.12:c.112C>G MANE Select	ENSP00000324856.6:p.Pro38Ala
ENST00000652231.1:c.112C>G	ENSP00000498804.1:p.Pro38Ala
ENST00000326873.11:c.112C>G	ENSP00000324856.6:p.Pro38Ala
ENST00000585748.2:c.-82-11392C>G	ENSP00000477641.1:n.-82-11392C>G
ENST00000585851.1:c.112C>G	ENSP00000467912.1:p.Pro38Ala
ENST00000586243.5:c.112C>G	ENSP00000467240.2:p.Pro38Ala
ENST00000589152.5:n.202C>G
ENST00000593219.5:c.112C>G	ENSP00000466610.1:p.Pro38Ala
NM_000455.4:c.112C>G , LRG_319t1:c.112C>G	NP_000446.1:p.Pro38Ala
XM_005259617.1:c.112C>G	XP_005259674.1:p.Pro38Ala
XM_005259618.3:c.112C>G	XP_005259675.1:p.Pro38Ala
XM_011528209.1:c.-242C>G	XP_011526511.1:n.-242C>G
XR_936204.1:n.737C>G
XM_005259617.3:c.112C>G	XP_005259674.1:p.Pro38Ala
XM_011528209.2:c.-242C>G	XP_011526511.1:n.-242C>G
XR_001753738.2:n.737C>G
XR_001753739.1:n.737C>G
XR_001753740.2:n.737C>G
NM_000455.5:c.112C>G MANE Select	NP_000446.1:p.Pro38Ala