Canonical Allele Identifier: CA504708548

Gene: STK11

Linked Data

• ClinVar Variation Id: 818760
• ClinVar RCV Id: RCV001010670
• dbSNP Id: rs1468066114
• MyVariant Identifiers: chr19:g.1226613G>A (hg19) ; chr19:g.1226614G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1226614G>A , CM000681.2:g.1226614G>A	GRCh38
NC_000019.9:g.1226613G>A , CM000681.1:g.1226613G>A	GRCh37
NC_000019.8:g.1177613G>A	NCBI36
NG_007460.2:g.42208G>A , LRG_319:g.42208G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.*2870G>A	ENSP00000490268.2:n.*2870G>A
ENST00000585748.3:c.897G>A	ENSP00000477641.2:p.Lys299=
ENST00000585851.2:c.1095G>A	ENSP00000467912.2:p.Lys365=
ENST00000326873.12:c.1269G>A MANE Select	ENSP00000324856.6:p.Lys423=
ENST00000326873.11:c.1269G>A	ENSP00000324856.6:p.Lys423=
ENST00000585465.2:n.3002G>A
ENST00000586243.5:c.1266G>A	ENSP00000467240.2:p.Lys422=
ENST00000589152.5:n.1967G>A
NM_000455.4:c.1269G>A , LRG_319t1:c.1269G>A	NP_000446.1:p.Lys423=
XM_005259617.1:c.1264G>A	XP_005259674.1:p.Asp422Asn
XM_011528209.1:c.1042G>A	XP_011526511.1:p.Asp348Asn
XM_005259617.3:c.1264G>A	XP_005259674.1:p.Asp422Asn
XM_011528209.2:c.1042G>A	XP_011526511.1:p.Asp348Asn
XR_001753738.2:n.2075G>A
XR_001753740.2:n.2045G>A
NM_000455.5:c.1269G>A MANE Select	NP_000446.1:p.Lys423=