Canonical Allele Identifier: CA891843674

Gene: STK11

Linked Data

• ClinVar Variation Id: 583088
• ClinVar RCV Id: RCV000707328
• dbSNP Id: rs1568689994
• MyVariant Identifiers: chr19:g.1207017_1207018del (hg19) ; chr19:g.1207018_1207019del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1207018_1207019del , CM000681.2:g.1207018_1207019del	GRCh38
NC_000019.9:g.1207017_1207018del , CM000681.1:g.1207017_1207018del	GRCh37
NC_000019.8:g.1158017_1158018del	NCBI36
NG_007460.2:g.22612_22613del , LRG_319:g.22612_22613del

Transcript Alleles

HGVS	Amino-acid change
ENST00000585465.3:c.105_106del	ENSP00000490268.2:p.Tyr36ProfsTer?
ENST00000585748.3:c.-82-11399_-82-11398del	ENSP00000477641.2:n.-82-11399_-82-11398de...
ENST00000585851.2:c.105_106del	ENSP00000467912.2:p.Tyr36ProfsTer?
ENST00000326873.12:c.105_106del MANE Select	ENSP00000324856.6:p.Tyr36ProfsTer?
ENST00000652231.1:c.105_106del	ENSP00000498804.1:p.Tyr36ProfsTer?
ENST00000326873.11:c.105_106del	ENSP00000324856.6:p.Tyr36ProfsTer?
ENST00000585748.2:c.-82-11399_-82-11398del	ENSP00000477641.1:n.-82-11399_-82-11398de...
ENST00000585851.1:c.105_106del	ENSP00000467912.1:p.Tyr36ProfsTer?
ENST00000586243.5:c.105_106del	ENSP00000467240.2:p.Tyr36ProfsTer?
ENST00000589152.5:n.195_196del
ENST00000593219.5:c.105_106del	ENSP00000466610.1:p.Tyr36ProfsTer?
NM_000455.4:c.105_106del , LRG_319t1:c.105_106del	NP_000446.1:p.Tyr36ProfsTer?
XM_005259617.1:c.105_106del	XP_005259674.1:p.Tyr36ProfsTer?
XM_005259618.3:c.105_106del	XP_005259675.1:p.Tyr36ProfsTer?
XM_011528209.1:c.-249_-248del	XP_011526511.1:n.-249_-248del
XR_936204.1:n.730_731del
XM_005259617.3:c.105_106del	XP_005259674.1:p.Tyr36ProfsTer?
XM_011528209.2:c.-249_-248del	XP_011526511.1:n.-249_-248del
XR_001753738.2:n.730_731del
XR_001753739.1:n.730_731del
XR_001753740.2:n.730_731del
NM_000455.5:c.105_106del MANE Select	NP_000446.1:p.Tyr36ProfsTer?