Canonical Allele Identifier: CA2739276341

Gene: STK11

Linked Data

• ClinVar Variation Id: 2913109
• ClinVar RCV Id: RCV003619051

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1222972T>C , CM000681.2:g.1222972T>C	GRCh38
NC_000019.9:g.1222971T>C , CM000681.1:g.1222971T>C	GRCh37
NC_000019.8:g.1173971T>C	NCBI36
NG_007460.2:g.38566T>C , LRG_319:g.38566T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.921-13T>C	ENSP00000490268.2:n.921-13T>C
ENST00000585748.3:c.549-13T>C	ENSP00000477641.2:n.549-13T>C
ENST00000585851.2:c.747-13T>C	ENSP00000467912.2:n.747-13T>C
ENST00000326873.12:c.921-13T>C MANE Select	ENSP00000324856.6:n.921-13T>C
ENST00000652231.1:c.921-13T>C	ENSP00000498804.1:n.921-13T>C
ENST00000326873.11:c.921-13T>C	ENSP00000324856.6:n.921-13T>C
ENST00000586243.5:c.921-13T>C	ENSP00000467240.2:n.921-13T>C
ENST00000589152.5:n.1619-13T>C
ENST00000591133.2:n.892-13T>C
NM_000455.4:c.921-13T>C , LRG_319t1:c.921-13T>C	NP_000446.1:n.921-13T>C
XM_005259617.1:c.921-13T>C	XP_005259674.1:n.921-13T>C
XM_005259618.3:c.921-13T>C	XP_005259675.1:n.921-13T>C
XM_011528209.1:c.699-13T>C	XP_011526511.1:n.699-13T>C
XR_936204.1:n.1697-13T>C
XM_005259617.3:c.921-13T>C	XP_005259674.1:n.921-13T>C
XM_011528209.2:c.699-13T>C	XP_011526511.1:n.699-13T>C
XR_001753738.2:n.1727-13T>C
XR_001753739.1:n.1727-13T>C
XR_001753740.2:n.1697-13T>C
NM_000455.5:c.921-13T>C MANE Select	NP_000446.1:n.921-13T>C