Canonical Allele Identifier: CA402953441

Gene: STK11

Linked Data

• ClinVar Variation Id: 922618
• ClinVar RCV Id: RCV001182798 ; RCV001321488
• dbSNP Id: rs878853983
• MyVariant Identifiers: chr19:g.1226506A>C (hg19) ; chr19:g.1226507A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1226507A>C , CM000681.2:g.1226507A>C	GRCh38
NC_000019.9:g.1226506A>C , CM000681.1:g.1226506A>C	GRCh37
NC_000019.8:g.1177506A>C	NCBI36
NG_007460.2:g.42101A>C , LRG_319:g.42101A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.*2763A>C	ENSP00000490268.2:n.*2763A>C
ENST00000585748.3:c.790A>C	ENSP00000477641.2:p.Lys264Gln
ENST00000585851.2:c.988A>C	ENSP00000467912.2:p.Lys330Gln
ENST00000326873.12:c.1162A>C MANE Select	ENSP00000324856.6:p.Lys388Gln
ENST00000326873.11:c.1162A>C	ENSP00000324856.6:p.Lys388Gln
ENST00000585465.2:n.2895A>C
ENST00000586243.5:c.1162A>C	ENSP00000467240.2:p.Lys388Gln
ENST00000589152.5:n.1860A>C
NM_000455.4:c.1162A>C , LRG_319t1:c.1162A>C	NP_000446.1:p.Lys388Gln
XM_005259617.1:c.1157A>C	XP_005259674.1:p.Gln386Pro
XM_011528209.1:c.935A>C	XP_011526511.1:p.Gln312Pro
XM_005259617.3:c.1157A>C	XP_005259674.1:p.Gln386Pro
XM_011528209.2:c.935A>C	XP_011526511.1:p.Gln312Pro
XR_001753738.2:n.1968A>C
XR_001753740.2:n.1938A>C
NM_000455.5:c.1162A>C MANE Select	NP_000446.1:p.Lys388Gln