Canonical Allele Identifier: CA2317593464

Gene: STK11

Linked Data

• dbSNP Id: rs2080819061
• gnomAD v4: 19-1226174-T-TG

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1226174_1226175insG , CM000681.2:g.1226174_1226175insG	GRCh38
NC_000019.9:g.1226173_1226174insG , CM000681.1:g.1226173_1226174insG	GRCh37
NC_000019.8:g.1177173_1177174insG	NCBI36
NG_007460.2:g.41768_41769insG , LRG_319:g.41768_41769insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.*2430_*2431insG	ENSP00000490268.2:n.*2430_*2431insG
ENST00000585748.3:c.737-280_737-279insG	ENSP00000477641.2:n.737-280_737-279insG
ENST00000585851.2:c.935-280_935-279insG	ENSP00000467912.2:n.935-280_935-279insG
ENST00000326873.12:c.1109-280_1109-279insG MANE Select	ENSP00000324856.6:n.1109-280_1109-279insG
ENST00000326873.11:c.1109-280_1109-279insG	ENSP00000324856.6:n.1109-280_1109-279insG
ENST00000585465.2:n.2562_2563insG
ENST00000586243.5:c.1109-280_1109-279insG	ENSP00000467240.2:n.1109-280_1109-279insG
ENST00000589152.5:n.1807-280_1807-279insG
NM_000455.4:c.1109-280_1109-279insG , LRG_319t1:c.1109-280_1109-279insG	NP_000446.1:n.1109-280_1109-279insG
XM_005259617.1:c.1109-285_1109-284insG	XP_005259674.1:n.1109-285_1109-284insG
XM_011528209.1:c.887-285_887-284insG	XP_011526511.1:n.887-285_887-284insG
XM_005259617.3:c.1109-285_1109-284insG	XP_005259674.1:n.1109-285_1109-284insG
XM_011528209.2:c.887-285_887-284insG	XP_011526511.1:n.887-285_887-284insG
XR_001753738.2:n.1915-280_1915-279insG
XR_001753740.2:n.1885-280_1885-279insG
NM_000455.5:c.1109-280_1109-279insG MANE Select	NP_000446.1:n.1109-280_1109-279insG