Canonical Allele Identifier: CA402953822

Gene: STK11

Linked Data

• ClinVar Variation Id: 2452002
• ClinVar RCV Id: RCV003187698
• dbSNP Id: rs749463771
• MyVariant Identifiers: chr19:g.1226566G>C (hg19) ; chr19:g.1226567G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1226567G>C , CM000681.2:g.1226567G>C	GRCh38
NC_000019.9:g.1226566G>C , CM000681.1:g.1226566G>C	GRCh37
NC_000019.8:g.1177566G>C	NCBI36
NG_007460.2:g.42161G>C , LRG_319:g.42161G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.*2823G>C	ENSP00000490268.2:n.*2823G>C
ENST00000585748.3:c.850G>C	ENSP00000477641.2:p.Gly284Arg
ENST00000585851.2:c.1048G>C	ENSP00000467912.2:p.Gly350Arg
ENST00000326873.12:c.1222G>C MANE Select	ENSP00000324856.6:p.Gly408Arg
ENST00000326873.11:c.1222G>C	ENSP00000324856.6:p.Gly408Arg
ENST00000585465.2:n.2955G>C
ENST00000586243.5:c.1222-1G>C	ENSP00000467240.2:n.1222-1G>C
ENST00000589152.5:n.1920G>C
NM_000455.4:c.1222G>C , LRG_319t1:c.1222G>C	NP_000446.1:p.Gly408Arg
XM_005259617.1:c.1217G>C	XP_005259674.1:p.Gly406Ala
XM_011528209.1:c.995G>C	XP_011526511.1:p.Gly332Ala
XM_005259617.3:c.1217G>C	XP_005259674.1:p.Gly406Ala
XM_011528209.2:c.995G>C	XP_011526511.1:p.Gly332Ala
XR_001753738.2:n.2028G>C
XR_001753740.2:n.1998G>C
NM_000455.5:c.1222G>C MANE Select	NP_000446.1:p.Gly408Arg