Canonical Allele Identifier: CA402953424

Gene: STK11

Linked Data

• gnomAD v4: 19-1226504-C-A
• MyVariant Identifiers: chr19:g.1226503C>A (hg19) ; chr19:g.1226504C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1226504C>A , CM000681.2:g.1226504C>A	GRCh38
NC_000019.9:g.1226503C>A , CM000681.1:g.1226503C>A	GRCh37
NC_000019.8:g.1177503C>A	NCBI36
NG_007460.2:g.42098C>A , LRG_319:g.42098C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.*2760C>A	ENSP00000490268.2:n.*2760C>A
ENST00000585748.3:c.787C>A	ENSP00000477641.2:p.Pro263Thr
ENST00000585851.2:c.985C>A	ENSP00000467912.2:p.Pro329Thr
ENST00000326873.12:c.1159C>A MANE Select	ENSP00000324856.6:p.Pro387Thr
ENST00000326873.11:c.1159C>A	ENSP00000324856.6:p.Pro387Thr
ENST00000585465.2:n.2892C>A
ENST00000586243.5:c.1159C>A	ENSP00000467240.2:p.Pro387Thr
ENST00000589152.5:n.1857C>A
NM_000455.4:c.1159C>A , LRG_319t1:c.1159C>A	NP_000446.1:p.Pro387Thr
XM_005259617.1:c.1154C>A	XP_005259674.1:p.Pro385His
XM_011528209.1:c.932C>A	XP_011526511.1:p.Pro311His
XM_005259617.3:c.1154C>A	XP_005259674.1:p.Pro385His
XM_011528209.2:c.932C>A	XP_011526511.1:p.Pro311His
XR_001753738.2:n.1965C>A
XR_001753740.2:n.1935C>A
NM_000455.5:c.1159C>A MANE Select	NP_000446.1:p.Pro387Thr