Canonical Allele Identifier: CA402954252

Gene: STK11

Linked Data

• dbSNP Id: rs2145436634
• gnomAD v4: 19-1226634-G-A
• MyVariant Identifiers: chr19:g.1226633G>A (hg19) ; chr19:g.1226634G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1226634G>A , CM000681.2:g.1226634G>A	GRCh38
NC_000019.9:g.1226633G>A , CM000681.1:g.1226633G>A	GRCh37
NC_000019.8:g.1177633G>A	NCBI36
NG_007460.2:g.42228G>A , LRG_319:g.42228G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000585465.3:c.*2890G>A	ENSP00000490268.2:n.*2890G>A
ENST00000585748.3:c.917G>A	ENSP00000477641.2:p.Cys306Tyr
ENST00000585851.2:c.1115G>A	ENSP00000467912.2:p.Cys372Tyr
ENST00000326873.12:c.1289G>A MANE Select	ENSP00000324856.6:p.Cys430Tyr
ENST00000326873.11:c.1289G>A	ENSP00000324856.6:p.Cys430Tyr
ENST00000585465.2:n.3022G>A
ENST00000586243.5:c.1286G>A	ENSP00000467240.2:p.Cys429Tyr
ENST00000589152.5:n.1987G>A
NM_000455.4:c.1289G>A , LRG_319t1:c.1289G>A	NP_000446.1:p.Cys430Tyr
XM_005259617.1:c.1284G>A	XP_005259674.1:p.Leu428=
XM_011528209.1:c.1062G>A	XP_011526511.1:p.Leu354=
XM_005259617.3:c.1284G>A	XP_005259674.1:p.Leu428=
XM_011528209.2:c.1062G>A	XP_011526511.1:p.Leu354=
XR_001753738.2:n.2095G>A
XR_001753740.2:n.2065G>A
NM_000455.5:c.1289G>A MANE Select	NP_000446.1:p.Cys430Tyr