Canonical Allele Identifier: CA2573155758

Gene: STK11

Linked Data

• ClinVar Variation Id: 1377341
• ClinVar RCV Id: RCV001889880
• dbSNP Id: rs2145424092

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1220369_1220370dup , CM000681.2:g.1220369_1220370dup	GRCh38
NC_000019.9:g.1220368_1220369dup , CM000681.1:g.1220368_1220369dup	GRCh37
NC_000019.8:g.1171368_1171369dup	NCBI36
NG_007460.2:g.35963_35964dup , LRG_319:g.35963_35964dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.465-4_465-3dup	ENSP00000490268.2:n.465-4_465-3dup
ENST00000585748.3:c.93-4_93-3dup	ENSP00000477641.2:n.93-4_93-3dup
ENST00000585851.2:c.291-4_291-3dup	ENSP00000467912.2:n.291-4_291-3dup
ENST00000326873.12:c.465-4_465-3dup MANE Select	ENSP00000324856.6:n.465-4_465-3dup
ENST00000652231.1:c.465-4_465-3dup	ENSP00000498804.1:n.465-4_465-3dup
ENST00000326873.11:c.465-4_465-3dup	ENSP00000324856.6:n.465-4_465-3dup
ENST00000585851.1:c.291-4_291-3dup	ENSP00000467912.1:n.291-4_291-3dup
ENST00000586243.5:c.465-4_465-3dup	ENSP00000467240.2:n.465-4_465-3dup
ENST00000586358.5:n.288-4_288-3dup
ENST00000589152.5:n.555-4_555-3dup
ENST00000591133.2:n.357_358dup
NM_000455.4:c.465-4_465-3dup , LRG_319t1:c.465-4_465-3dup	NP_000446.1:n.465-4_465-3dup
XM_005259617.1:c.465-4_465-3dup	XP_005259674.1:n.465-4_465-3dup
XM_005259618.3:c.465-4_465-3dup	XP_005259675.1:n.465-4_465-3dup
XM_011528209.1:c.243-4_243-3dup	XP_011526511.1:n.243-4_243-3dup
XR_936204.1:n.1090-4_1090-3dup
XM_005259617.3:c.465-4_465-3dup	XP_005259674.1:n.465-4_465-3dup
XM_011528209.2:c.243-4_243-3dup	XP_011526511.1:n.243-4_243-3dup
XR_001753738.2:n.1090-4_1090-3dup
XR_001753739.1:n.1090-4_1090-3dup
XR_001753740.2:n.1090-4_1090-3dup
NM_000455.5:c.465-4_465-3dup MANE Select	NP_000446.1:n.465-4_465-3dup