Canonical Allele Identifier: CA504706590

Gene: STK11

Linked Data

• ClinVar Variation Id: 1115378
• ClinVar RCV Id: RCV001443371
• dbSNP Id: rs2145422154
• MyVariant Identifiers: chr19:g.1219326T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1219327T>C , CM000681.2:g.1219327T>C	GRCh38
NC_000019.9:g.1219326T>C , CM000681.1:g.1219326T>C	GRCh37
NC_000019.8:g.1170326T>C	NCBI36
NG_007460.2:g.34921T>C , LRG_319:g.34921T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000585465.3:c.378T>C	ENSP00000490268.2:p.Tyr126=
ENST00000585748.3:c.6T>C	ENSP00000477641.2:p.Tyr2=
ENST00000585851.2:c.291-1046T>C	ENSP00000467912.2:n.291-1046T>C
ENST00000326873.12:c.378T>C MANE Select	ENSP00000324856.6:p.Tyr126=
ENST00000652231.1:c.378T>C	ENSP00000498804.1:p.Tyr126=
ENST00000326873.11:c.378T>C	ENSP00000324856.6:p.Tyr126=
ENST00000585748.2:c.6T>C	ENSP00000477641.1:p.Tyr2=
ENST00000585851.1:c.291-1046T>C	ENSP00000467912.1:n.291-1046T>C
ENST00000586243.5:c.378T>C	ENSP00000467240.2:p.Tyr126=
ENST00000586358.5:n.201T>C
ENST00000589152.5:n.468T>C
ENST00000593219.5:c.*203T>C	ENSP00000466610.1:n.*203T>C
NM_000455.4:c.378T>C , LRG_319t1:c.378T>C	NP_000446.1:p.Tyr126=
XM_005259617.1:c.378T>C	XP_005259674.1:p.Tyr126=
XM_005259618.3:c.378T>C	XP_005259675.1:p.Tyr126=
XM_011528209.1:c.156T>C	XP_011526511.1:p.Tyr52=
XR_936204.1:n.1003T>C
XM_005259617.3:c.378T>C	XP_005259674.1:p.Tyr126=
XM_011528209.2:c.156T>C	XP_011526511.1:p.Tyr52=
XR_001753738.2:n.1003T>C
XR_001753739.1:n.1003T>C
XR_001753740.2:n.1003T>C
NM_000455.5:c.378T>C MANE Select	NP_000446.1:p.Tyr126=