Canonical Allele Identifier: CA10581019

Gene: STK11

Linked Data

• ClinVar Variation Id: 403774
• ClinVar RCV Id: RCV000220434 ; RCV000463989 ; RCV001653818
• dbSNP Id: rs876659704
• MyVariant Identifiers: chr19:g.1226605_1226606delinsCT (hg19) ; chr19:g.1226606_1226607delinsCT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1226606_1226607delinsCT , CM000681.2:g.1226606_1226607delinsCT	GRCh38
NC_000019.9:g.1226605_1226606delinsCT , CM000681.1:g.1226605_1226606delinsCT	GRCh37
NC_000019.8:g.1177605_1177606delinsCT	NCBI36
NG_007460.2:g.42200_42201delinsCT , LRG_319:g.42200_42201delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.*2862_*2863delinsCT	ENSP00000490268.2:n.*2862_*2863delinsCT
ENST00000585748.3:c.889_890delinsCT	ENSP00000477641.2:p.Ser297Leu
ENST00000585851.2:c.1087_1088delinsCT	ENSP00000467912.2:p.Ser363Leu
ENST00000326873.12:c.1261_1262delinsCT MANE Select	ENSP00000324856.6:p.Ser421Leu
ENST00000326873.11:c.1261_1262delinsCT	ENSP00000324856.6:p.Ser421Leu
ENST00000585465.2:n.2994_2995delinsCT
ENST00000586243.5:c.1258_1259delinsCT	ENSP00000467240.2:p.Ser420Leu
ENST00000589152.5:n.1959_1960delinsCT
NM_000455.4:c.1261_1262delinsCT , LRG_319t1:c.1261_1262delinsCT	NP_000446.1:p.Ser421Leu
XM_005259617.1:c.1256_1257delinsCT	XP_005259674.1:p.Gln419Pro
XM_011528209.1:c.1034_1035delinsCT	XP_011526511.1:p.Gln345Pro
XM_005259617.3:c.1256_1257delinsCT	XP_005259674.1:p.Gln419Pro
XM_011528209.2:c.1034_1035delinsCT	XP_011526511.1:p.Gln345Pro
XR_001753738.2:n.2067_2068delinsCT
XR_001753740.2:n.2037_2038delinsCT
NM_000455.5:c.1261_1262delinsCT MANE Select	NP_000446.1:p.Ser421Leu