Canonical Allele Identifier: CA915951603

Gene: STK11

Linked Data

• ClinVar Variation Id: 818564
• ClinVar RCV Id: RCV001010267 ; RCV001317359
• dbSNP Id: rs1599932256

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1226537_1226538delinsTT , CM000681.2:g.1226537_1226538delinsTT	GRCh38
NC_000019.9:g.1226536_1226537delinsTT , CM000681.1:g.1226536_1226537delinsTT	GRCh37
NC_000019.8:g.1177536_1177537delinsTT	NCBI36
NG_007460.2:g.42131_42132delinsTT , LRG_319:g.42131_42132delinsTT

Transcript Alleles

HGVS	Amino-acid change
ENST00000585465.3:c.*2793_*2794delinsTT	ENSP00000490268.2:n.*2793_*2794delinsTT
ENST00000585748.3:c.820_821delinsTT	ENSP00000477641.2:p.Ala274Leu
ENST00000585851.2:c.1018_1019delinsTT	ENSP00000467912.2:p.Ala340Leu
ENST00000326873.12:c.1192_1193delinsTT MANE Select	ENSP00000324856.6:p.Ala398Leu
ENST00000326873.11:c.1192_1193delinsTT	ENSP00000324856.6:p.Ala398Leu
ENST00000585465.2:n.2925_2926delinsTT
ENST00000586243.5:c.1192_1193delinsTT	ENSP00000467240.2:p.Ala398Leu
ENST00000589152.5:n.1890_1891delinsTT
NM_000455.4:c.1192_1193delinsTT , LRG_319t1:c.1192_1193delinsTT	NP_000446.1:p.Ala398Leu
XM_005259617.1:c.1187_1188delinsTT	XP_005259674.1:p.Gly396Val
XM_011528209.1:c.965_966delinsTT	XP_011526511.1:p.Gly322Val
XM_005259617.3:c.1187_1188delinsTT	XP_005259674.1:p.Gly396Val
XM_011528209.2:c.965_966delinsTT	XP_011526511.1:p.Gly322Val
XR_001753738.2:n.1998_1999delinsTT
XR_001753740.2:n.1968_1969delinsTT
NM_000455.5:c.1192_1193delinsTT MANE Select	NP_000446.1:p.Ala398Leu