Canonical Allele Identifier: CA658799089

Gene: STK11

Linked Data

• ClinVar Variation Id: 527838
• ClinVar RCV Id: RCV000632838
• dbSNP Id: rs1555738656
• MyVariant Identifiers: chr19:g.1221272_1221273dup (hg19) ; chr19:g.1221273_1221274dup (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1221273_1221274dup , CM000681.2:g.1221273_1221274dup	GRCh38
NC_000019.9:g.1221272_1221273dup , CM000681.1:g.1221272_1221273dup	GRCh37
NC_000019.8:g.1172272_1172273dup	NCBI36
NG_007460.2:g.36867_36868dup , LRG_319:g.36867_36868dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000585465.3:c.795_796dup	ENSP00000490268.2:p.Asn266ArgfsTer22
ENST00000585748.3:c.423_424dup	ENSP00000477641.2:p.Asn142ArgfsTer22
ENST00000585851.2:c.621_622dup	ENSP00000467912.2:p.Asn208ArgfsTer22
ENST00000326873.12:c.795_796dup MANE Select	ENSP00000324856.6:p.Asn266ArgfsTer22
ENST00000652231.1:c.795_796dup	ENSP00000498804.1:p.Asn266ArgfsTer22
ENST00000326873.11:c.795_796dup	ENSP00000324856.6:p.Asn266ArgfsTer22
ENST00000586243.5:c.795_796dup	ENSP00000467240.2:p.Asn266ArgfsTer22
ENST00000586358.5:n.693_694dup
ENST00000589152.5:n.885_886dup
ENST00000591133.2:n.766_767dup
NM_000455.4:c.795_796dup , LRG_319t1:c.795_796dup	NP_000446.1:p.Asn266ArgfsTer22
XM_005259617.1:c.795_796dup	XP_005259674.1:p.Asn266ArgfsTer22
XM_005259618.3:c.795_796dup	XP_005259675.1:p.Asn266ArgfsTer22
XM_011528209.1:c.573_574dup	XP_011526511.1:p.Asn192ArgfsTer22
XR_936204.1:n.1420_1421dup
XM_005259617.3:c.795_796dup	XP_005259674.1:p.Asn266ArgfsTer22
XM_011528209.2:c.573_574dup	XP_011526511.1:p.Asn192ArgfsTer22
XR_001753738.2:n.1420_1421dup
XR_001753739.1:n.1420_1421dup
XR_001753740.2:n.1420_1421dup
NM_000455.5:c.795_796dup MANE Select	NP_000446.1:p.Asn266ArgfsTer22