Canonical Allele Identifier: CA658656792

Gene: STK11

Linked Data

• ClinVar Variation Id: 458030
• ClinVar RCV Id: RCV000560077 ; RCV000562727 ; RCV002476112
• dbSNP Id: rs1555740261

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1226607_1226608delinsAT , CM000681.2:g.1226607_1226608delinsAT	GRCh38
NC_000019.9:g.1226606_1226607delinsAT , CM000681.1:g.1226606_1226607delinsAT	GRCh37
NC_000019.8:g.1177606_1177607delinsAT	NCBI36
NG_007460.2:g.42201_42202delinsAT , LRG_319:g.42201_42202delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.*2863_*2864delinsAT	ENSP00000490268.2:n.*2863_*2864delinsAT
ENST00000585748.3:c.890_891delinsAT	ENSP00000477641.2:p.Ser297Asn
ENST00000585851.2:c.1088_1089delinsAT	ENSP00000467912.2:p.Ser363Asn
ENST00000326873.12:c.1262_1263delinsAT MANE Select	ENSP00000324856.6:p.Ser421Asn
ENST00000326873.11:c.1262_1263delinsAT	ENSP00000324856.6:p.Ser421Asn
ENST00000585465.2:n.2995_2996delinsAT
ENST00000586243.5:c.1259_1260delinsAT	ENSP00000467240.2:p.Ser420Asn
ENST00000589152.5:n.1960_1961delinsAT
NM_000455.4:c.1262_1263delinsAT , LRG_319t1:c.1262_1263delinsAT	NP_000446.1:p.Ser421Asn
XM_005259617.1:c.1257_1258delinsAT	XP_005259674.1:p.Gln420Ter
XM_011528209.1:c.1035_1036delinsAT	XP_011526511.1:p.Gln346Ter
XM_005259617.3:c.1257_1258delinsAT	XP_005259674.1:p.Gln420Ter
XM_011528209.2:c.1035_1036delinsAT	XP_011526511.1:p.Gln346Ter
XR_001753738.2:n.2068_2069delinsAT
XR_001753740.2:n.2038_2039delinsAT
NM_000455.5:c.1262_1263delinsAT MANE Select	NP_000446.1:p.Ser421Asn