Canonical Allele Identifier: CA891862954

Gene: STK11

Linked Data

• ClinVar Variation Id: 591841
• ClinVar RCV Id: RCV000723023
• dbSNP Id: rs1568717494

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1226605_1226635del , CM000681.2:g.1226605_1226635del	GRCh38
NC_000019.9:g.1226604_1226634del , CM000681.1:g.1226604_1226634del	GRCh37
NC_000019.8:g.1177604_1177634del	NCBI36
NG_007460.2:g.42199_42229del , LRG_319:g.42199_42229del

Transcript Alleles

HGVS	Amino-acid change
ENST00000585465.3:c.*2861_*2891del	ENSP00000490268.2:n.*2861_*2891del
ENST00000585748.3:c.888_918del	ENSP00000477641.2:p.Lys299SerfsTer?
ENST00000585851.2:c.1086_1116del	ENSP00000467912.2:p.Lys365SerfsTer?
ENST00000326873.12:c.1260_1290del MANE Select	ENSP00000324856.6:p.Lys423SerfsTer?
ENST00000326873.11:c.1260_1290del	ENSP00000324856.6:p.Lys423SerfsTer?
ENST00000585465.2:n.2993_3023del
ENST00000586243.5:c.1257_1287del	ENSP00000467240.2:p.Lys422SerfsTer?
ENST00000589152.5:n.1958_1988del
NM_000455.4:c.1260_1290del , LRG_319t1:c.1260_1290del	NP_000446.1:p.Lys423SerfsTer?
XM_005259617.1:c.1255_1285del	XP_005259674.1:p.Gln419LysfsTer4
XM_011528209.1:c.1033_1063del	XP_011526511.1:p.Gln345LysfsTer4
XM_005259617.3:c.1255_1285del	XP_005259674.1:p.Gln419LysfsTer4
XM_011528209.2:c.1033_1063del	XP_011526511.1:p.Gln345LysfsTer4
XR_001753738.2:n.2066_2096del
XR_001753740.2:n.2036_2066del
NM_000455.5:c.1260_1290del MANE Select	NP_000446.1:p.Lys423SerfsTer?