Canonical Allele Identifier: CA402954105

Gene: STK11

Linked Data

• ClinVar Variation Id: 3231735
• ClinVar RCV Id: RCV004518450
• MyVariant Identifiers: chr19:g.1226607C>G (hg19) ; chr19:g.1226608C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1226608C>G , CM000681.2:g.1226608C>G	GRCh38
NC_000019.9:g.1226607C>G , CM000681.1:g.1226607C>G	GRCh37
NC_000019.8:g.1177607C>G	NCBI36
NG_007460.2:g.42202C>G , LRG_319:g.42202C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.*2864C>G	ENSP00000490268.2:n.*2864C>G
ENST00000585748.3:c.891C>G	ENSP00000477641.2:p.Ser297Arg
ENST00000585851.2:c.1089C>G	ENSP00000467912.2:p.Ser363Arg
ENST00000326873.12:c.1263C>G MANE Select	ENSP00000324856.6:p.Ser421Arg
ENST00000326873.11:c.1263C>G	ENSP00000324856.6:p.Ser421Arg
ENST00000585465.2:n.2996C>G
ENST00000586243.5:c.1260C>G	ENSP00000467240.2:p.Ser420Arg
ENST00000589152.5:n.1961C>G
NM_000455.4:c.1263C>G , LRG_319t1:c.1263C>G	NP_000446.1:p.Ser421Arg
XM_005259617.1:c.1258C>G	XP_005259674.1:p.Gln420Glu
XM_011528209.1:c.1036C>G	XP_011526511.1:p.Gln346Glu
XM_005259617.3:c.1258C>G	XP_005259674.1:p.Gln420Glu
XM_011528209.2:c.1036C>G	XP_011526511.1:p.Gln346Glu
XR_001753738.2:n.2069C>G
XR_001753740.2:n.2039C>G
NM_000455.5:c.1263C>G MANE Select	NP_000446.1:p.Ser421Arg