Canonical Allele Identifier: CA2695198105

Gene: STK11

Linked Data

• ClinVar Variation Id: 2679059
• ClinVar RCV Id: RCV003466420

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1226562del , CM000681.2:g.1226562del	GRCh38
NC_000019.9:g.1226561del , CM000681.1:g.1226561del	GRCh37
NC_000019.8:g.1177561del	NCBI36
NG_007460.2:g.42156del , LRG_319:g.42156del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.*2818del	ENSP00000490268.2:n.*2818del
ENST00000585748.3:c.845del	ENSP00000477641.2:p.Ala282GlyfsTer?
ENST00000585851.2:c.1043del	ENSP00000467912.2:p.Ala348GlyfsTer?
ENST00000326873.12:c.1217del MANE Select	ENSP00000324856.6:p.Ala406GlyfsTer?
ENST00000326873.11:c.1217del	ENSP00000324856.6:p.Ala406GlyfsTer?
ENST00000585465.2:n.2950del
ENST00000586243.5:c.1217del	ENSP00000467240.2:p.Ala406GlyfsTer?
ENST00000589152.5:n.1915del
NM_000455.4:c.1217del , LRG_319t1:c.1217del	NP_000446.1:p.Ala406GlyfsTer?
XM_005259617.1:c.1212del	XP_005259674.1:p.Gly405GlufsTer28
XM_011528209.1:c.990del	XP_011526511.1:p.Gly331GlufsTer28
XM_005259617.3:c.1212del	XP_005259674.1:p.Gly405GlufsTer28
XM_011528209.2:c.990del	XP_011526511.1:p.Gly331GlufsTer28
XR_001753738.2:n.2023del
XR_001753740.2:n.1993del
NM_000455.5:c.1217del MANE Select	NP_000446.1:p.Ala406GlyfsTer?