Canonical Allele Identifier: CA402953450

Gene: STK11

Linked Data

• dbSNP Id: rs756877141
• MyVariant Identifiers: chr19:g.1226507A>C (hg19) ; chr19:g.1226508A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1226508A>C , CM000681.2:g.1226508A>C	GRCh38
NC_000019.9:g.1226507A>C , CM000681.1:g.1226507A>C	GRCh37
NC_000019.8:g.1177507A>C	NCBI36
NG_007460.2:g.42102A>C , LRG_319:g.42102A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.*2764A>C	ENSP00000490268.2:n.*2764A>C
ENST00000585748.3:c.791A>C	ENSP00000477641.2:p.Lys264Thr
ENST00000585851.2:c.989A>C	ENSP00000467912.2:p.Lys330Thr
ENST00000326873.12:c.1163A>C MANE Select	ENSP00000324856.6:p.Lys388Thr
ENST00000326873.11:c.1163A>C	ENSP00000324856.6:p.Lys388Thr
ENST00000585465.2:n.2896A>C
ENST00000586243.5:c.1163A>C	ENSP00000467240.2:p.Lys388Thr
ENST00000589152.5:n.1861A>C
NM_000455.4:c.1163A>C , LRG_319t1:c.1163A>C	NP_000446.1:p.Lys388Thr
XM_005259617.1:c.1158A>C	XP_005259674.1:p.Gln386His
XM_011528209.1:c.936A>C	XP_011526511.1:p.Gln312His
XM_005259617.3:c.1158A>C	XP_005259674.1:p.Gln386His
XM_011528209.2:c.936A>C	XP_011526511.1:p.Gln312His
XR_001753738.2:n.1969A>C
XR_001753740.2:n.1939A>C
NM_000455.5:c.1163A>C MANE Select	NP_000446.1:p.Lys388Thr