Canonical Allele Identifier: CA402954156

Gene: STK11

Linked Data

• ClinVar Variation Id: 3231736
• ClinVar RCV Id: RCV004518451
• dbSNP Id: rs2145436527
• MyVariant Identifiers: chr19:g.1226614A>C (hg19) ; chr19:g.1226615A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1226615A>C , CM000681.2:g.1226615A>C	GRCh38
NC_000019.9:g.1226614A>C , CM000681.1:g.1226614A>C	GRCh37
NC_000019.8:g.1177614A>C	NCBI36
NG_007460.2:g.42209A>C , LRG_319:g.42209A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.*2871A>C	ENSP00000490268.2:n.*2871A>C
ENST00000585748.3:c.898A>C	ENSP00000477641.2:p.Ile300Leu
ENST00000585851.2:c.1096A>C	ENSP00000467912.2:p.Ile366Leu
ENST00000326873.12:c.1270A>C MANE Select	ENSP00000324856.6:p.Ile424Leu
ENST00000326873.11:c.1270A>C	ENSP00000324856.6:p.Ile424Leu
ENST00000585465.2:n.3003A>C
ENST00000586243.5:c.1267A>C	ENSP00000467240.2:p.Ile423Leu
ENST00000589152.5:n.1968A>C
NM_000455.4:c.1270A>C , LRG_319t1:c.1270A>C	NP_000446.1:p.Ile424Leu
XM_005259617.1:c.1265A>C	XP_005259674.1:p.Asp422Ala
XM_011528209.1:c.1043A>C	XP_011526511.1:p.Asp348Ala
XM_005259617.3:c.1265A>C	XP_005259674.1:p.Asp422Ala
XM_011528209.2:c.1043A>C	XP_011526511.1:p.Asp348Ala
XR_001753738.2:n.2076A>C
XR_001753740.2:n.2046A>C
NM_000455.5:c.1270A>C MANE Select	NP_000446.1:p.Ile424Leu