Canonical Allele Identifier: CA915951591

Gene: STK11

Linked Data

• ClinVar Variation Id: 704207
• ClinVar RCV Id: RCV001498337
• dbSNP Id: rs1599928242
• gnomAD v4: 19-1221942-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1221942T>C , CM000681.2:g.1221942T>C	GRCh38
NC_000019.9:g.1221941T>C , CM000681.1:g.1221941T>C	GRCh37
NC_000019.8:g.1172941T>C	NCBI36
NG_007460.2:g.37536T>C , LRG_319:g.37536T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.863-7T>C	ENSP00000490268.2:n.863-7T>C
ENST00000585748.3:c.491-7T>C	ENSP00000477641.2:n.491-7T>C
ENST00000585851.2:c.689-7T>C	ENSP00000467912.2:n.689-7T>C
ENST00000326873.12:c.863-7T>C MANE Select	ENSP00000324856.6:n.863-7T>C
ENST00000652231.1:c.863-7T>C	ENSP00000498804.1:n.863-7T>C
ENST00000326873.11:c.863-7T>C	ENSP00000324856.6:n.863-7T>C
ENST00000586243.5:c.863-7T>C	ENSP00000467240.2:n.863-7T>C
ENST00000586358.5:n.761-7T>C
ENST00000589152.5:n.1554T>C
ENST00000591133.2:n.834-7T>C
NM_000455.4:c.863-7T>C , LRG_319t1:c.863-7T>C	NP_000446.1:n.863-7T>C
XM_005259617.1:c.863-7T>C	XP_005259674.1:n.863-7T>C
XM_005259618.3:c.863-7T>C	XP_005259675.1:n.863-7T>C
XM_011528209.1:c.641-7T>C	XP_011526511.1:n.641-7T>C
XR_936204.1:n.1639-7T>C
XM_005259617.3:c.863-7T>C	XP_005259674.1:n.863-7T>C
XM_011528209.2:c.641-7T>C	XP_011526511.1:n.641-7T>C
XR_001753738.2:n.1669-7T>C
XR_001753739.1:n.1669-7T>C
XR_001753740.2:n.1639-7T>C
NM_000455.5:c.863-7T>C MANE Select	NP_000446.1:n.863-7T>C