Canonical Allele Identifier: CA402954126

Gene: STK11

Linked Data

• ClinVar Variation Id: 1369838
• ClinVar RCV Id: RCV001870845
• dbSNP Id: rs1555740268
• MyVariant Identifiers: chr19:g.1226611A>C (hg19) ; chr19:g.1226612A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1226612A>C , CM000681.2:g.1226612A>C	GRCh38
NC_000019.9:g.1226611A>C , CM000681.1:g.1226611A>C	GRCh37
NC_000019.8:g.1177611A>C	NCBI36
NG_007460.2:g.42206A>C , LRG_319:g.42206A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.*2868A>C	ENSP00000490268.2:n.*2868A>C
ENST00000585748.3:c.895A>C	ENSP00000477641.2:p.Lys299Gln
ENST00000585851.2:c.1093A>C	ENSP00000467912.2:p.Lys365Gln
ENST00000326873.12:c.1267A>C MANE Select	ENSP00000324856.6:p.Lys423Gln
ENST00000326873.11:c.1267A>C	ENSP00000324856.6:p.Lys423Gln
ENST00000585465.2:n.3000A>C
ENST00000586243.5:c.1264A>C	ENSP00000467240.2:p.Lys422Gln
ENST00000589152.5:n.1965A>C
NM_000455.4:c.1267A>C , LRG_319t1:c.1267A>C	NP_000446.1:p.Lys423Gln
XM_005259617.1:c.1262A>C	XP_005259674.1:p.Gln421Pro
XM_011528209.1:c.1040A>C	XP_011526511.1:p.Gln347Pro
XM_005259617.3:c.1262A>C	XP_005259674.1:p.Gln421Pro
XM_011528209.2:c.1040A>C	XP_011526511.1:p.Gln347Pro
XR_001753738.2:n.2073A>C
XR_001753740.2:n.2043A>C
NM_000455.5:c.1267A>C MANE Select	NP_000446.1:p.Lys423Gln