Canonical Allele Identifier: CA504708533

Gene: STK11

Linked Data

• dbSNP Id: rs1436178098
• gnomAD v2: 19-1226541-G-A
• gnomAD v4: 19-1226542-G-A
• MyVariant Identifiers: chr19:g.1226541G>A (hg19) ; chr19:g.1226542G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1226542G>A , CM000681.2:g.1226542G>A	GRCh38
NC_000019.9:g.1226541G>A , CM000681.1:g.1226541G>A	GRCh37
NC_000019.8:g.1177541G>A	NCBI36
NG_007460.2:g.42136G>A , LRG_319:g.42136G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.*2798G>A	ENSP00000490268.2:n.*2798G>A
ENST00000585748.3:c.825G>A	ENSP00000477641.2:p.Gln275=
ENST00000585851.2:c.1023G>A	ENSP00000467912.2:p.Gln341=
ENST00000326873.12:c.1197G>A MANE Select	ENSP00000324856.6:p.Gln399=
ENST00000326873.11:c.1197G>A	ENSP00000324856.6:p.Gln399=
ENST00000585465.2:n.2930G>A
ENST00000586243.5:c.1197G>A	ENSP00000467240.2:p.Gln399=
ENST00000589152.5:n.1895G>A
NM_000455.4:c.1197G>A , LRG_319t1:c.1197G>A	NP_000446.1:p.Gln399=
XM_005259617.1:c.1192G>A	XP_005259674.1:p.Ala398Thr
XM_011528209.1:c.970G>A	XP_011526511.1:p.Ala324Thr
XM_005259617.3:c.1192G>A	XP_005259674.1:p.Ala398Thr
XM_011528209.2:c.970G>A	XP_011526511.1:p.Ala324Thr
XR_001753738.2:n.2003G>A
XR_001753740.2:n.1973G>A
NM_000455.5:c.1197G>A MANE Select	NP_000446.1:p.Gln399=