Canonical Allele Identifier: CA16616012

Gene: STK11

Linked Data

• ClinVar Variation Id: 403780
• ClinVar RCV Id: RCV000474608
• dbSNP Id: rs397518443
• MyVariant Identifiers: chr19:g.1222998_1222999del (hg19) ; chr19:g.1222999_1223000del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1222999_1223000del , CM000681.2:g.1222999_1223000del	GRCh38
NC_000019.9:g.1222998_1222999del , CM000681.1:g.1222998_1222999del	GRCh37
NC_000019.8:g.1173998_1173999del	NCBI36
NG_007460.2:g.38593_38594del , LRG_319:g.38593_38594del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.935_936del	ENSP00000490268.2:p.Lys312ThrfsTer5
ENST00000585748.3:c.563_564del	ENSP00000477641.2:p.Lys188ThrfsTer5
ENST00000585851.2:c.761_762del	ENSP00000467912.2:p.Lys254ThrfsTer5
ENST00000326873.12:c.935_936del MANE Select	ENSP00000324856.6:p.Lys312ThrfsTer5
ENST00000652231.1:c.935_936del	ENSP00000498804.1:p.Lys312ThrfsTer5
ENST00000326873.11:c.935_936del	ENSP00000324856.6:p.Lys312ThrfsTer5
ENST00000586243.5:c.935_936del	ENSP00000467240.2:p.Lys312ThrfsTer5
ENST00000589152.5:n.1633_1634del
ENST00000591133.2:n.906_907del
NM_000455.4:c.935_936del , LRG_319t1:c.935_936del	NP_000446.1:p.Lys312ThrfsTer5
XM_005259617.1:c.935_936del	XP_005259674.1:p.Lys312ThrfsTer5
XM_005259618.3:c.935_936del	XP_005259675.1:p.Lys312ThrfsTer5
XM_011528209.1:c.713_714del	XP_011526511.1:p.Lys238ThrfsTer5
XR_936204.1:n.1711_1712del
XM_005259617.3:c.935_936del	XP_005259674.1:p.Lys312ThrfsTer5
XM_011528209.2:c.713_714del	XP_011526511.1:p.Lys238ThrfsTer5
XR_001753738.2:n.1741_1742del
XR_001753739.1:n.1741_1742del
XR_001753740.2:n.1711_1712del
NM_000455.5:c.935_936del MANE Select	NP_000446.1:p.Lys312ThrfsTer5