Canonical Allele Identifier: CA631034289

Gene: STK11

Linked Data

• dbSNP Id: rs1568717819
• gnomAD v2: 19-1226674-C-CGGGGCCCGGGT
• gnomAD v3: 19-1226675-C-CGGGGCCCGGGT
• gnomAD v4: 19-1226675-C-CGGGGCCCGGGT
• MyVariant Identifiers: chr19:g.1226674_1226675insGGGGCCCGGGT (hg19) ; chr19:g.1226675_1226676insGGGGCCCGGGT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1226681_1226691dup , CM000681.2:g.1226681_1226691dup	GRCh38
NC_000019.9:g.1226680_1226690dup , CM000681.1:g.1226680_1226690dup	GRCh37
NC_000019.8:g.1177680_1177690dup	NCBI36
NG_007460.2:g.42275_42285dup , LRG_319:g.42275_42285dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.*2919+18_*2919+28dup	ENSP00000490268.2:n.*2919+18_*2919+28dup
ENST00000585748.3:c.*16+18_*16+28dup	ENSP00000477641.2:n.*16+18_*16+28dup
ENST00000585851.2:c.*16+18_*16+28dup	ENSP00000467912.2:n.*16+18_*16+28dup
ENST00000326873.12:c.*16+18_*16+28dup MANE Select	ENSP00000324856.6:n.*16+18_*16+28dup
ENST00000326873.11:c.*16+18_*16+28dup	ENSP00000324856.6:n.*16+18_*16+28dup
ENST00000585465.2:n.3051+18_3051+28dup
ENST00000586243.5:c.*16+18_*16+28dup	ENSP00000467240.2:n.*16+18_*16+28dup
ENST00000589152.5:n.2034_2044dup
NM_000455.4:c.*16+18_*16+28dup , LRG_319t1:c.*16+18_*16+28dup	NP_000446.1:n.*16+18_*16+28dup
XM_005259617.1:c.1313+18_1313+28dup	XP_005259674.1:n.1313+18_1313+28dup
XM_011528209.1:c.1091+18_1091+28dup	XP_011526511.1:n.1091+18_1091+28dup
XM_005259617.3:c.1313+18_1313+28dup	XP_005259674.1:n.1313+18_1313+28dup
XM_011528209.2:c.1091+18_1091+28dup	XP_011526511.1:n.1091+18_1091+28dup
XR_001753738.2:n.2124+18_2124+28dup
XR_001753740.2:n.2094+18_2094+28dup
NM_000455.5:c.*16+18_*16+28dup MANE Select	NP_000446.1:n.*16+18_*16+28dup