Canonical Allele Identifier: CA992494134

Gene: STK11

Linked Data

• dbSNP Id: rs1057522868
• gnomAD v3: 19-1226656-G-T
• gnomAD v4: 19-1226656-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1226656G>T , CM000681.2:g.1226656G>T	GRCh38
NC_000019.9:g.1226655G>T , CM000681.1:g.1226655G>T	GRCh37
NC_000019.8:g.1177655G>T	NCBI36
NG_007460.2:g.42250G>T , LRG_319:g.42250G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.*2912G>T	ENSP00000490268.2:n.*2912G>T
ENST00000585748.3:c.*9G>T	ENSP00000477641.2:n.*9G>T
ENST00000585851.2:c.*9G>T	ENSP00000467912.2:n.*9G>T
ENST00000326873.12:c.*9G>T MANE Select	ENSP00000324856.6:n.*9G>T
ENST00000326873.11:c.*9G>T	ENSP00000324856.6:n.*9G>T
ENST00000585465.2:n.3044G>T
ENST00000586243.5:c.*9G>T	ENSP00000467240.2:n.*9G>T
ENST00000589152.5:n.2009G>T
NM_000455.4:c.*9G>T , LRG_319t1:c.*9G>T	NP_000446.1:n.*9G>T
XM_005259617.1:c.1306G>T	XP_005259674.1:p.Ala436Ser
XM_011528209.1:c.1084G>T	XP_011526511.1:p.Ala362Ser
XM_005259617.3:c.1306G>T	XP_005259674.1:p.Ala436Ser
XM_011528209.2:c.1084G>T	XP_011526511.1:p.Ala362Ser
XR_001753738.2:n.2117G>T
XR_001753740.2:n.2087G>T
NM_000455.5:c.*9G>T MANE Select	NP_000446.1:n.*9G>T