Canonical Allele Identifier: CA402953611

Gene: STK11

Linked Data

• ClinVar Variation Id: 1415907
• ClinVar RCV Id: RCV001933320 ; RCV003365554
• dbSNP Id: rs587780008
• gnomAD v4: 19-1226534-G-A
• MyVariant Identifiers: chr19:g.1226533G>A (hg19) ; chr19:g.1226534G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1226534G>A , CM000681.2:g.1226534G>A	GRCh38
NC_000019.9:g.1226533G>A , CM000681.1:g.1226533G>A	GRCh37
NC_000019.8:g.1177533G>A	NCBI36
NG_007460.2:g.42128G>A , LRG_319:g.42128G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.*2790G>A	ENSP00000490268.2:n.*2790G>A
ENST00000585748.3:c.817G>A	ENSP00000477641.2:p.Ala273Thr
ENST00000585851.2:c.1015G>A	ENSP00000467912.2:p.Ala339Thr
ENST00000326873.12:c.1189G>A MANE Select	ENSP00000324856.6:p.Ala397Thr
ENST00000326873.11:c.1189G>A	ENSP00000324856.6:p.Ala397Thr
ENST00000585465.2:n.2922G>A
ENST00000586243.5:c.1189G>A	ENSP00000467240.2:p.Ala397Thr
ENST00000589152.5:n.1887G>A
NM_000455.4:c.1189G>A , LRG_319t1:c.1189G>A	NP_000446.1:p.Ala397Thr
XM_005259617.1:c.1184G>A	XP_005259674.1:p.Gly395Asp
XM_011528209.1:c.962G>A	XP_011526511.1:p.Gly321Asp
XM_005259617.3:c.1184G>A	XP_005259674.1:p.Gly395Asp
XM_011528209.2:c.962G>A	XP_011526511.1:p.Gly321Asp
XR_001753738.2:n.1995G>A
XR_001753740.2:n.1965G>A
NM_000455.5:c.1189G>A MANE Select	NP_000446.1:p.Ala397Thr