Canonical Allele Identifier: CA402953503

Gene: STK11

Linked Data

• dbSNP Id: rs1214125670
• MyVariant Identifiers: chr19:g.1226515T>A (hg19) ; chr19:g.1226516T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1226516T>A , CM000681.2:g.1226516T>A	GRCh38
NC_000019.9:g.1226515T>A , CM000681.1:g.1226515T>A	GRCh37
NC_000019.8:g.1177515T>A	NCBI36
NG_007460.2:g.42110T>A , LRG_319:g.42110T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.*2772T>A	ENSP00000490268.2:n.*2772T>A
ENST00000585748.3:c.799T>A	ENSP00000477641.2:p.Cys267Ser
ENST00000585851.2:c.997T>A	ENSP00000467912.2:p.Cys333Ser
ENST00000326873.12:c.1171T>A MANE Select	ENSP00000324856.6:p.Cys391Ser
ENST00000326873.11:c.1171T>A	ENSP00000324856.6:p.Cys391Ser
ENST00000585465.2:n.2904T>A
ENST00000586243.5:c.1171T>A	ENSP00000467240.2:p.Cys391Ser
ENST00000589152.5:n.1869T>A
NM_000455.4:c.1171T>A , LRG_319t1:c.1171T>A	NP_000446.1:p.Cys391Ser
XM_005259617.1:c.1166T>A	XP_005259674.1:p.Val389Glu
XM_011528209.1:c.944T>A	XP_011526511.1:p.Val315Glu
XM_005259617.3:c.1166T>A	XP_005259674.1:p.Val389Glu
XM_011528209.2:c.944T>A	XP_011526511.1:p.Val315Glu
XR_001753738.2:n.1977T>A
XR_001753740.2:n.1947T>A
NM_000455.5:c.1171T>A MANE Select	NP_000446.1:p.Cys391Ser