Canonical Allele Identifier: CA402953253

Gene: STK11

Linked Data

• dbSNP Id: rs2145435903
• MyVariant Identifiers: chr19:g.1226478T>A (hg19) ; chr19:g.1226479T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1226479T>A , CM000681.2:g.1226479T>A	GRCh38
NC_000019.9:g.1226478T>A , CM000681.1:g.1226478T>A	GRCh37
NC_000019.8:g.1177478T>A	NCBI36
NG_007460.2:g.42073T>A , LRG_319:g.42073T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.*2735T>A	ENSP00000490268.2:n.*2735T>A
ENST00000585748.3:c.762T>A	ENSP00000477641.2:p.Ser254Arg
ENST00000585851.2:c.960T>A	ENSP00000467912.2:p.Ser320Arg
ENST00000326873.12:c.1134T>A MANE Select	ENSP00000324856.6:p.Ser378Arg
ENST00000326873.11:c.1134T>A	ENSP00000324856.6:p.Ser378Arg
ENST00000585465.2:n.2867T>A
ENST00000586243.5:c.1134T>A	ENSP00000467240.2:p.Ser378Arg
ENST00000589152.5:n.1832T>A
NM_000455.4:c.1134T>A , LRG_319t1:c.1134T>A	NP_000446.1:p.Ser378Arg
XM_005259617.1:c.1129T>A	XP_005259674.1:p.Ser377Thr
XM_011528209.1:c.907T>A	XP_011526511.1:p.Ser303Thr
XM_005259617.3:c.1129T>A	XP_005259674.1:p.Ser377Thr
XM_011528209.2:c.907T>A	XP_011526511.1:p.Ser303Thr
XR_001753738.2:n.1940T>A
XR_001753740.2:n.1910T>A
NM_000455.5:c.1134T>A MANE Select	NP_000446.1:p.Ser378Arg