Canonical Allele Identifier: CA16608852

Gene: STK11

Linked Data

• ClinVar Variation Id: 390387
• ClinVar RCV Id: RCV000432723 ; RCV000582343 ; RCV001808824
• dbSNP Id: rs1057523753
• gnomAD v4: 19-1226653-G-A
• MyVariant Identifiers: chr19:g.1226652G>A (hg19) ; chr19:g.1226653G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1226653G>A , CM000681.2:g.1226653G>A	GRCh38
NC_000019.9:g.1226652G>A , CM000681.1:g.1226652G>A	GRCh37
NC_000019.8:g.1177652G>A	NCBI36
NG_007460.2:g.42247G>A , LRG_319:g.42247G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.*2909G>A	ENSP00000490268.2:n.*2909G>A
ENST00000585748.3:c.*6G>A	ENSP00000477641.2:n.*6G>A
ENST00000585851.2:c.*6G>A	ENSP00000467912.2:n.*6G>A
ENST00000326873.12:c.*6G>A MANE Select	ENSP00000324856.6:n.*6G>A
ENST00000326873.11:c.*6G>A	ENSP00000324856.6:n.*6G>A
ENST00000585465.2:n.3041G>A
ENST00000586243.5:c.*6G>A	ENSP00000467240.2:n.*6G>A
ENST00000589152.5:n.2006G>A
NM_000455.4:c.*6G>A , LRG_319t1:c.*6G>A	NP_000446.1:n.*6G>A
XM_005259617.1:c.1303G>A	XP_005259674.1:p.Ala435Thr
XM_011528209.1:c.1081G>A	XP_011526511.1:p.Ala361Thr
XM_005259617.3:c.1303G>A	XP_005259674.1:p.Ala435Thr
XM_011528209.2:c.1081G>A	XP_011526511.1:p.Ala361Thr
XR_001753738.2:n.2114G>A
XR_001753740.2:n.2084G>A
NM_000455.5:c.*6G>A MANE Select	NP_000446.1:n.*6G>A