Canonical Allele Identifier: CA2581946002

Gene: STK11

Linked Data

• dbSNP Id: rs2145435323
• gnomAD v3: 19-1226231-A-G
• gnomAD v4: 19-1226231-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1226231A>G , CM000681.2:g.1226231A>G	GRCh38
NC_000019.9:g.1226230A>G , CM000681.1:g.1226230A>G	GRCh37
NC_000019.8:g.1177230A>G	NCBI36
NG_007460.2:g.41825A>G , LRG_319:g.41825A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.*2487A>G	ENSP00000490268.2:n.*2487A>G
ENST00000585748.3:c.737-223A>G	ENSP00000477641.2:n.737-223A>G
ENST00000585851.2:c.935-223A>G	ENSP00000467912.2:n.935-223A>G
ENST00000326873.12:c.1109-223A>G MANE Select	ENSP00000324856.6:n.1109-223A>G
ENST00000326873.11:c.1109-223A>G	ENSP00000324856.6:n.1109-223A>G
ENST00000585465.2:n.2619A>G
ENST00000586243.5:c.1109-223A>G	ENSP00000467240.2:n.1109-223A>G
ENST00000589152.5:n.1807-223A>G
NM_000455.4:c.1109-223A>G , LRG_319t1:c.1109-223A>G	NP_000446.1:n.1109-223A>G
XM_005259617.1:c.1109-228A>G	XP_005259674.1:n.1109-228A>G
XM_011528209.1:c.887-228A>G	XP_011526511.1:n.887-228A>G
XM_005259617.3:c.1109-228A>G	XP_005259674.1:n.1109-228A>G
XM_011528209.2:c.887-228A>G	XP_011526511.1:n.887-228A>G
XR_001753738.2:n.1915-223A>G
XR_001753740.2:n.1885-223A>G
NM_000455.5:c.1109-223A>G MANE Select	NP_000446.1:n.1109-223A>G