Canonical Allele Identifier: CA2317589049

Gene: STK11

Linked Data

• ClinVar Variation Id: 952489
• ClinVar RCV Id: RCV002366011
• dbSNP Id: rs2080765043

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1219317_1219318del , CM000681.2:g.1219317_1219318del	GRCh38
NC_000019.9:g.1219316_1219317del , CM000681.1:g.1219316_1219317del	GRCh37
NC_000019.8:g.1170316_1170317del	NCBI36
NG_007460.2:g.34911_34912del , LRG_319:g.34911_34912del

Transcript Alleles

HGVS	Amino-acid change
ENST00000585465.3:c.375-7_375-6del	ENSP00000490268.2:n.375-7_375-6del
ENST00000585748.3:c.3-7_3-6del	ENSP00000477641.2:n.3-7_3-6del
ENST00000585851.2:c.291-1056_291-1055del	ENSP00000467912.2:n.291-1056_291-1055del
ENST00000326873.12:c.375-7_375-6del MANE Select	ENSP00000324856.6:n.375-7_375-6del
ENST00000652231.1:c.375-7_375-6del	ENSP00000498804.1:n.375-7_375-6del
ENST00000326873.11:c.375-7_375-6del	ENSP00000324856.6:n.375-7_375-6del
ENST00000585748.2:c.3-7_3-6del	ENSP00000477641.1:n.3-7_3-6del
ENST00000585851.1:c.291-1056_291-1055del	ENSP00000467912.1:n.291-1056_291-1055del
ENST00000586243.5:c.375-7_375-6del	ENSP00000467240.2:n.375-7_375-6del
ENST00000586358.5:n.198-7_198-6del
ENST00000589152.5:n.465-7_465-6del
ENST00000593219.5:c.*200-7_*200-6del	ENSP00000466610.1:n.*200-7_*200-6del
NM_000455.4:c.375-7_375-6del , LRG_319t1:c.375-7_375-6del	NP_000446.1:n.375-7_375-6del
XM_005259617.1:c.375-7_375-6del	XP_005259674.1:n.375-7_375-6del
XM_005259618.3:c.375-7_375-6del	XP_005259675.1:n.375-7_375-6del
XM_011528209.1:c.153-7_153-6del	XP_011526511.1:n.153-7_153-6del
XR_936204.1:n.1000-7_1000-6del
XM_005259617.3:c.375-7_375-6del	XP_005259674.1:n.375-7_375-6del
XM_011528209.2:c.153-7_153-6del	XP_011526511.1:n.153-7_153-6del
XR_001753738.2:n.1000-7_1000-6del
XR_001753739.1:n.1000-7_1000-6del
XR_001753740.2:n.1000-7_1000-6del
NM_000455.5:c.375-7_375-6del MANE Select	NP_000446.1:n.375-7_375-6del