Canonical Allele Identifier: CA504706167

Gene: STK11

Linked Data

• ClinVar Variation Id: 1542893
• ClinVar RCV Id: RCV002167596
• dbSNP Id: rs2145405165
• MyVariant Identifiers: chr19:g.1207060C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1207061C>T , CM000681.2:g.1207061C>T	GRCh38
NC_000019.9:g.1207060C>T , CM000681.1:g.1207060C>T	GRCh37
NC_000019.8:g.1158060C>T	NCBI36
NG_007460.2:g.22655C>T , LRG_319:g.22655C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.148C>T	ENSP00000490268.2:p.Leu50=
ENST00000585748.3:c.-82-11356C>T	ENSP00000477641.2:n.-82-11356C>T
ENST00000585851.2:c.148C>T	ENSP00000467912.2:p.Leu50=
ENST00000326873.12:c.148C>T MANE Select	ENSP00000324856.6:p.Leu50=
ENST00000652231.1:c.148C>T	ENSP00000498804.1:p.Leu50=
ENST00000326873.11:c.148C>T	ENSP00000324856.6:p.Leu50=
ENST00000585748.2:c.-82-11356C>T	ENSP00000477641.1:n.-82-11356C>T
ENST00000585851.1:c.148C>T	ENSP00000467912.1:p.Leu50=
ENST00000586243.5:c.148C>T	ENSP00000467240.2:p.Leu50=
ENST00000589152.5:n.238C>T
ENST00000593219.5:c.148C>T	ENSP00000466610.1:p.Leu50=
NM_000455.4:c.148C>T , LRG_319t1:c.148C>T	NP_000446.1:p.Leu50=
XM_005259617.1:c.148C>T	XP_005259674.1:p.Leu50=
XM_005259618.3:c.148C>T	XP_005259675.1:p.Leu50=
XM_011528209.1:c.-206C>T	XP_011526511.1:n.-206C>T
XR_936204.1:n.773C>T
XM_005259617.3:c.148C>T	XP_005259674.1:p.Leu50=
XM_011528209.2:c.-206C>T	XP_011526511.1:n.-206C>T
XR_001753738.2:n.773C>T
XR_001753739.1:n.773C>T
XR_001753740.2:n.773C>T
NM_000455.5:c.148C>T MANE Select	NP_000446.1:p.Leu50=