Canonical Allele Identifier: CA2317593711

Gene: STK11

Linked Data

• ClinVar Variation Id: 1016148
• ClinVar RCV Id: RCV001315112
• dbSNP Id: rs2080822675

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1226538_1226564del , CM000681.2:g.1226538_1226564del	GRCh38
NC_000019.9:g.1226537_1226563del , CM000681.1:g.1226537_1226563del	GRCh37
NC_000019.8:g.1177537_1177563del	NCBI36
NG_007460.2:g.42132_42158del , LRG_319:g.42132_42158del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.*2794_*2820del	ENSP00000490268.2:n.*2794_*2820del
ENST00000585748.3:c.821_847del	ENSP00000477641.2:p.Ala274_Ala282del
ENST00000585851.2:c.1019_1045del	ENSP00000467912.2:p.Ala340_Ala348del
ENST00000326873.12:c.1193_1219del MANE Select	ENSP00000324856.6:p.Ala398_Ala406del
ENST00000326873.11:c.1193_1219del	ENSP00000324856.6:p.Ala398_Ala406del
ENST00000585465.2:n.2926_2952del
ENST00000586243.5:c.1193_1219del	ENSP00000467240.2:p.Ala398_Ala406del
ENST00000589152.5:n.1891_1917del
NM_000455.4:c.1193_1219del , LRG_319t1:c.1193_1219del	NP_000446.1:p.Ala398_Ala406del
XM_005259617.1:c.1188_1214del	XP_005259674.1:p.Ala397_Gly405del
XM_011528209.1:c.966_992del	XP_011526511.1:p.Ala323_Gly331del
XM_005259617.3:c.1188_1214del	XP_005259674.1:p.Ala397_Gly405del
XM_011528209.2:c.966_992del	XP_011526511.1:p.Ala323_Gly331del
XR_001753738.2:n.1999_2025del
XR_001753740.2:n.1969_1995del
NM_000455.5:c.1193_1219del MANE Select	NP_000446.1:p.Ala398_Ala406del