Canonical Allele Identifier: CA402953729

Gene: STK11

Linked Data

• ClinVar Variation Id: 1467284
• ClinVar RCV Id: RCV001970371
• dbSNP Id: rs587781633
• COSMIC: COSM327302
• MyVariant Identifiers: chr19:g.1226552A>T (hg19) ; chr19:g.1226553A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1226553A>T , CM000681.2:g.1226553A>T	GRCh38
NC_000019.9:g.1226552A>T , CM000681.1:g.1226552A>T	GRCh37
NC_000019.8:g.1177552A>T	NCBI36
NG_007460.2:g.42147A>T , LRG_319:g.42147A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.*2809A>T	ENSP00000490268.2:n.*2809A>T
ENST00000585748.3:c.836A>T	ENSP00000477641.2:p.Lys279Ile
ENST00000585851.2:c.1034A>T	ENSP00000467912.2:p.Lys345Ile
ENST00000326873.12:c.1208A>T MANE Select	ENSP00000324856.6:p.Lys403Ile
ENST00000326873.11:c.1208A>T	ENSP00000324856.6:p.Lys403Ile
ENST00000585465.2:n.2941A>T
ENST00000586243.5:c.1208A>T	ENSP00000467240.2:p.Lys403Ile
ENST00000589152.5:n.1906A>T
NM_000455.4:c.1208A>T , LRG_319t1:c.1208A>T	NP_000446.1:p.Lys403Ile
XM_005259617.1:c.1203A>T	XP_005259674.1:p.Gln401His
XM_011528209.1:c.981A>T	XP_011526511.1:p.Gln327His
XM_005259617.3:c.1203A>T	XP_005259674.1:p.Gln401His
XM_011528209.2:c.981A>T	XP_011526511.1:p.Gln327His
XR_001753738.2:n.2014A>T
XR_001753740.2:n.1984A>T
NM_000455.5:c.1208A>T MANE Select	NP_000446.1:p.Lys403Ile