Canonical Allele Identifier: CA992494168

Gene: STK11

Linked Data

• dbSNP Id: rs2080825091
• gnomAD v3: 19-1226672-CGGCGGGGCCCGGGTGGGGCA-C
• gnomAD v4: 19-1226672-CGGCGGGGCCCGGGTGGGGCA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1226673_1226692del , CM000681.2:g.1226673_1226692del	GRCh38
NC_000019.9:g.1226672_1226691del , CM000681.1:g.1226672_1226691del	GRCh37
NC_000019.8:g.1177672_1177691del	NCBI36
NG_007460.2:g.42267_42286del , LRG_319:g.42267_42286del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.*2919+10_*2919+29del	ENSP00000490268.2:n.*2919+10_*2919+29del
ENST00000585748.3:c.*16+10_*16+29del	ENSP00000477641.2:n.*16+10_*16+29del
ENST00000585851.2:c.*16+10_*16+29del	ENSP00000467912.2:n.*16+10_*16+29del
ENST00000326873.12:c.*16+10_*16+29del MANE Select	ENSP00000324856.6:n.*16+10_*16+29del
ENST00000326873.11:c.*16+10_*16+29del	ENSP00000324856.6:n.*16+10_*16+29del
ENST00000585465.2:n.3051+10_3051+29del
ENST00000586243.5:c.*16+10_*16+29del	ENSP00000467240.2:n.*16+10_*16+29del
ENST00000589152.5:n.2026_2045del
NM_000455.4:c.*16+10_*16+29del , LRG_319t1:c.*16+10_*16+29del	NP_000446.1:n.*16+10_*16+29del
XM_005259617.1:c.1313+10_1313+29del	XP_005259674.1:n.1313+10_1313+29del
XM_011528209.1:c.1091+10_1091+29del	XP_011526511.1:n.1091+10_1091+29del
XM_005259617.3:c.1313+10_1313+29del	XP_005259674.1:n.1313+10_1313+29del
XM_011528209.2:c.1091+10_1091+29del	XP_011526511.1:n.1091+10_1091+29del
XR_001753738.2:n.2124+10_2124+29del
XR_001753740.2:n.2094+10_2094+29del
NM_000455.5:c.*16+10_*16+29del MANE Select	NP_000446.1:n.*16+10_*16+29del