Canonical Allele Identifier: CA2697555610

Gene: STK11

Linked Data

• ClinVar Variation Id: 2739269
• ClinVar RCV Id: RCV003508943

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1226534_1226535delinsTT , CM000681.2:g.1226534_1226535delinsTT	GRCh38
NC_000019.9:g.1226533_1226534delinsTT , CM000681.1:g.1226533_1226534delinsTT	GRCh37
NC_000019.8:g.1177533_1177534delinsTT	NCBI36
NG_007460.2:g.42128_42129delinsTT , LRG_319:g.42128_42129delinsTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.*2790_*2791delinsTT	ENSP00000490268.2:n.*2790_*2791delinsTT
ENST00000585748.3:c.817_818delinsTT	ENSP00000477641.2:p.Ala273Leu
ENST00000585851.2:c.1015_1016delinsTT	ENSP00000467912.2:p.Ala339Leu
ENST00000326873.12:c.1189_1190delinsTT MANE Select	ENSP00000324856.6:p.Ala397Leu
ENST00000326873.11:c.1189_1190delinsTT	ENSP00000324856.6:p.Ala397Leu
ENST00000585465.2:n.2922_2923delinsTT
ENST00000586243.5:c.1189_1190delinsTT	ENSP00000467240.2:p.Ala397Leu
ENST00000589152.5:n.1887_1888delinsTT
NM_000455.4:c.1189_1190delinsTT , LRG_319t1:c.1189_1190delinsTT	NP_000446.1:p.Ala397Leu
XM_005259617.1:c.1184_1185delinsTT	XP_005259674.1:p.Gly395Val
XM_011528209.1:c.962_963delinsTT	XP_011526511.1:p.Gly321Val
XM_005259617.3:c.1184_1185delinsTT	XP_005259674.1:p.Gly395Val
XM_011528209.2:c.962_963delinsTT	XP_011526511.1:p.Gly321Val
XR_001753738.2:n.1995_1996delinsTT
XR_001753740.2:n.1965_1966delinsTT
NM_000455.5:c.1189_1190delinsTT MANE Select	NP_000446.1:p.Ala397Leu