Canonical Allele Identifier: CA2499225348

Gene: STK11

Linked Data

• ClinVar Variation Id: 1073558
• ClinVar RCV Id: RCV001386590
• dbSNP Id: rs2145425162

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1220623_1220636del , CM000681.2:g.1220623_1220636del	GRCh38
NC_000019.9:g.1220622_1220635del , CM000681.1:g.1220622_1220635del	GRCh37
NC_000019.8:g.1171622_1171635del	NCBI36
NG_007460.2:g.36217_36230del , LRG_319:g.36217_36230del

Transcript Alleles

HGVS	Amino-acid change
ENST00000585465.3:c.640_653del	ENSP00000490268.2:p.Gln214PhefsTer?
ENST00000585748.3:c.268_281del	ENSP00000477641.2:p.Gln90PhefsTer?
ENST00000585851.2:c.466_479del	ENSP00000467912.2:p.Gln156PhefsTer?
ENST00000326873.12:c.640_653del MANE Select	ENSP00000324856.6:p.Gln214PhefsTer?
ENST00000652231.1:c.640_653del	ENSP00000498804.1:p.Gln214PhefsTer?
ENST00000326873.11:c.640_653del	ENSP00000324856.6:p.Gln214PhefsTer?
ENST00000586243.5:c.640_653del	ENSP00000467240.2:p.Gln214PhefsTer?
ENST00000586358.5:n.538_551del
ENST00000589152.5:n.730_743del
ENST00000591133.2:n.611_624del
NM_000455.4:c.640_653del , LRG_319t1:c.640_653del	NP_000446.1:p.Gln214PhefsTer?
XM_005259617.1:c.640_653del	XP_005259674.1:p.Gln214PhefsTer?
XM_005259618.3:c.640_653del	XP_005259675.1:p.Gln214PhefsTer?
XM_011528209.1:c.418_431del	XP_011526511.1:p.Gln140PhefsTer?
XR_936204.1:n.1265_1278del
XM_005259617.3:c.640_653del	XP_005259674.1:p.Gln214PhefsTer?
XM_011528209.2:c.418_431del	XP_011526511.1:p.Gln140PhefsTer?
XR_001753738.2:n.1265_1278del
XR_001753739.1:n.1265_1278del
XR_001753740.2:n.1265_1278del
NM_000455.5:c.640_653del MANE Select	NP_000446.1:p.Gln214PhefsTer?