Canonical Allele Identifier: CA504708353

Gene: STK11

Linked Data

• dbSNP Id: rs2145435827
• MyVariant Identifiers: chr19:g.1226460C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1226461C>T , CM000681.2:g.1226461C>T	GRCh38
NC_000019.9:g.1226460C>T , CM000681.1:g.1226460C>T	GRCh37
NC_000019.8:g.1177460C>T	NCBI36
NG_007460.2:g.42055C>T , LRG_319:g.42055C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.*2717C>T	ENSP00000490268.2:n.*2717C>T
ENST00000585748.3:c.744C>T	ENSP00000477641.2:p.Val248=
ENST00000585851.2:c.942C>T	ENSP00000467912.2:p.Val314=
ENST00000326873.12:c.1116C>T MANE Select	ENSP00000324856.6:p.Val372=
ENST00000326873.11:c.1116C>T	ENSP00000324856.6:p.Val372=
ENST00000585465.2:n.2849C>T
ENST00000586243.5:c.1116C>T	ENSP00000467240.2:p.Val372=
ENST00000589152.5:n.1814C>T
NM_000455.4:c.1116C>T , LRG_319t1:c.1116C>T	NP_000446.1:p.Val372=
XM_005259617.1:c.1111C>T	XP_005259674.1:p.Pro371Ser
XM_011528209.1:c.889C>T	XP_011526511.1:p.Pro297Ser
XM_005259617.3:c.1111C>T	XP_005259674.1:p.Pro371Ser
XM_011528209.2:c.889C>T	XP_011526511.1:p.Pro297Ser
XR_001753738.2:n.1922C>T
XR_001753740.2:n.1892C>T
NM_000455.5:c.1116C>T MANE Select	NP_000446.1:p.Val372=