Canonical Allele Identifier: CA048583

Gene: STK11

Linked Data

• ClinVar Variation Id: 256207
• ClinVar RCV Id: RCV000249987 ; RCV000574507 ; RCV000632865
• dbSNP Id: rs776823114
• ExAC: 19:1220708 G / T
• gnomAD v2: 19-1220708-G-T
• gnomAD v4: 19-1220709-G-T
• MyVariant Identifiers: chr19:g.1220708G>T (hg19) ; chr19:g.1220709G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1220709G>T , CM000681.2:g.1220709G>T	GRCh38
NC_000019.9:g.1220708G>T , CM000681.1:g.1220708G>T	GRCh37
NC_000019.8:g.1171708G>T	NCBI36
NG_007460.2:g.36303G>T , LRG_319:g.36303G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.726G>T	ENSP00000490268.2:p.Gly242=
ENST00000585748.3:c.354G>T	ENSP00000477641.2:p.Gly118=
ENST00000585851.2:c.552G>T	ENSP00000467912.2:p.Gly184=
ENST00000326873.12:c.726G>T MANE Select	ENSP00000324856.6:p.Gly242=
ENST00000652231.1:c.726G>T	ENSP00000498804.1:p.Gly242=
ENST00000326873.11:c.726G>T	ENSP00000324856.6:p.Gly242=
ENST00000586243.5:c.726G>T	ENSP00000467240.2:p.Gly242=
ENST00000586358.5:n.624G>T
ENST00000589152.5:n.816G>T
ENST00000591133.2:n.697G>T
NM_000455.4:c.726G>T , LRG_319t1:c.726G>T	NP_000446.1:p.Gly242=
XM_005259617.1:c.726G>T	XP_005259674.1:p.Gly242=
XM_005259618.3:c.726G>T	XP_005259675.1:p.Gly242=
XM_011528209.1:c.504G>T	XP_011526511.1:p.Gly168=
XR_936204.1:n.1351G>T
XM_005259617.3:c.726G>T	XP_005259674.1:p.Gly242=
XM_011528209.2:c.504G>T	XP_011526511.1:p.Gly168=
XR_001753738.2:n.1351G>T
XR_001753739.1:n.1351G>T
XR_001753740.2:n.1351G>T
NM_000455.5:c.726G>T MANE Select	NP_000446.1:p.Gly242=