Canonical Allele Identifier: CA992493671

Gene: STK11

Linked Data

• dbSNP Id: rs2080819466
• gnomAD v3: 19-1226218-CGTG-C
• gnomAD v4: 19-1226218-CGTG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1226223_1226225del , CM000681.2:g.1226223_1226225del	GRCh38
NC_000019.9:g.1226222_1226224del , CM000681.1:g.1226222_1226224del	GRCh37
NC_000019.8:g.1177222_1177224del	NCBI36
NG_007460.2:g.41817_41819del , LRG_319:g.41817_41819del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.*2479_*2481del	ENSP00000490268.2:n.*2479_*2481del
ENST00000585748.3:c.737-231_737-229del	ENSP00000477641.2:n.737-231_737-229del
ENST00000585851.2:c.935-231_935-229del	ENSP00000467912.2:n.935-231_935-229del
ENST00000326873.12:c.1109-231_1109-229del MANE Select	ENSP00000324856.6:n.1109-231_1109-229del
ENST00000326873.11:c.1109-231_1109-229del	ENSP00000324856.6:n.1109-231_1109-229del
ENST00000585465.2:n.2611_2613del
ENST00000586243.5:c.1109-231_1109-229del	ENSP00000467240.2:n.1109-231_1109-229del
ENST00000589152.5:n.1807-231_1807-229del
NM_000455.4:c.1109-231_1109-229del , LRG_319t1:c.1109-231_1109-229del	NP_000446.1:n.1109-231_1109-229del
XM_005259617.1:c.1109-236_1109-234del	XP_005259674.1:n.1109-236_1109-234del
XM_011528209.1:c.887-236_887-234del	XP_011526511.1:n.887-236_887-234del
XM_005259617.3:c.1109-236_1109-234del	XP_005259674.1:n.1109-236_1109-234del
XM_011528209.2:c.887-236_887-234del	XP_011526511.1:n.887-236_887-234del
XR_001753738.2:n.1915-231_1915-229del
XR_001753740.2:n.1885-231_1885-229del
NM_000455.5:c.1109-231_1109-229del MANE Select	NP_000446.1:n.1109-231_1109-229del