Canonical Allele Identifier: CA402953607

Gene: STK11

Linked Data

• ClinVar Variation Id: 818540
• ClinVar RCV Id: RCV001010229
• dbSNP Id: rs1599932241
• MyVariant Identifiers: chr19:g.1226532G>C (hg19) ; chr19:g.1226533G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1226533G>C , CM000681.2:g.1226533G>C	GRCh38
NC_000019.9:g.1226532G>C , CM000681.1:g.1226532G>C	GRCh37
NC_000019.8:g.1177532G>C	NCBI36
NG_007460.2:g.42127G>C , LRG_319:g.42127G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.*2789G>C	ENSP00000490268.2:n.*2789G>C
ENST00000585748.3:c.816G>C	ENSP00000477641.2:p.Glu272Asp
ENST00000585851.2:c.1014G>C	ENSP00000467912.2:p.Glu338Asp
ENST00000326873.12:c.1188G>C MANE Select	ENSP00000324856.6:p.Glu396Asp
ENST00000326873.11:c.1188G>C	ENSP00000324856.6:p.Glu396Asp
ENST00000585465.2:n.2921G>C
ENST00000586243.5:c.1188G>C	ENSP00000467240.2:p.Glu396Asp
ENST00000589152.5:n.1886G>C
NM_000455.4:c.1188G>C , LRG_319t1:c.1188G>C	NP_000446.1:p.Glu396Asp
XM_005259617.1:c.1183G>C	XP_005259674.1:p.Gly395Arg
XM_011528209.1:c.961G>C	XP_011526511.1:p.Gly321Arg
XM_005259617.3:c.1183G>C	XP_005259674.1:p.Gly395Arg
XM_011528209.2:c.961G>C	XP_011526511.1:p.Gly321Arg
XR_001753738.2:n.1994G>C
XR_001753740.2:n.1964G>C
NM_000455.5:c.1188G>C MANE Select	NP_000446.1:p.Glu396Asp