Canonical Allele Identifier: CA631033948

Gene: STK11

Linked Data

• dbSNP Id: rs1416251693
• gnomAD v2: 19-1226232-A-G
• gnomAD v4: 19-1226233-A-G
• MyVariant Identifiers: chr19:g.1226232A>G (hg19) ; chr19:g.1226233A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1226233A>G , CM000681.2:g.1226233A>G	GRCh38
NC_000019.9:g.1226232A>G , CM000681.1:g.1226232A>G	GRCh37
NC_000019.8:g.1177232A>G	NCBI36
NG_007460.2:g.41827A>G , LRG_319:g.41827A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.*2489A>G	ENSP00000490268.2:n.*2489A>G
ENST00000585748.3:c.737-221A>G	ENSP00000477641.2:n.737-221A>G
ENST00000585851.2:c.935-221A>G	ENSP00000467912.2:n.935-221A>G
ENST00000326873.12:c.1109-221A>G MANE Select	ENSP00000324856.6:n.1109-221A>G
ENST00000326873.11:c.1109-221A>G	ENSP00000324856.6:n.1109-221A>G
ENST00000585465.2:n.2621A>G
ENST00000586243.5:c.1109-221A>G	ENSP00000467240.2:n.1109-221A>G
ENST00000589152.5:n.1807-221A>G
NM_000455.4:c.1109-221A>G , LRG_319t1:c.1109-221A>G	NP_000446.1:n.1109-221A>G
XM_005259617.1:c.1109-226A>G	XP_005259674.1:n.1109-226A>G
XM_011528209.1:c.887-226A>G	XP_011526511.1:n.887-226A>G
XM_005259617.3:c.1109-226A>G	XP_005259674.1:n.1109-226A>G
XM_011528209.2:c.887-226A>G	XP_011526511.1:n.887-226A>G
XR_001753738.2:n.1915-221A>G
XR_001753740.2:n.1885-221A>G
NM_000455.5:c.1109-221A>G MANE Select	NP_000446.1:n.1109-221A>G