Canonical Allele Identifier: CA504707351

Gene: STK11

Linked Data

• MyVariant Identifiers: chr19:g.1221335G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1221336G>T , CM000681.2:g.1221336G>T	GRCh38
NC_000019.9:g.1221335G>T , CM000681.1:g.1221335G>T	GRCh37
NC_000019.8:g.1172335G>T	NCBI36
NG_007460.2:g.36930G>T , LRG_319:g.36930G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.858G>T	ENSP00000490268.2:p.Leu286=
ENST00000585748.3:c.486G>T	ENSP00000477641.2:p.Leu162=
ENST00000585851.2:c.684G>T	ENSP00000467912.2:p.Leu228=
ENST00000326873.12:c.858G>T MANE Select	ENSP00000324856.6:p.Leu286=
ENST00000652231.1:c.858G>T	ENSP00000498804.1:p.Leu286=
ENST00000326873.11:c.858G>T	ENSP00000324856.6:p.Leu286=
ENST00000586243.5:c.858G>T	ENSP00000467240.2:p.Leu286=
ENST00000586358.5:n.756G>T
ENST00000589152.5:n.948G>T
ENST00000591133.2:n.829G>T
NM_000455.4:c.858G>T , LRG_319t1:c.858G>T	NP_000446.1:p.Leu286=
XM_005259617.1:c.858G>T	XP_005259674.1:p.Leu286=
XM_005259618.3:c.858G>T	XP_005259675.1:p.Leu286=
XM_011528209.1:c.636G>T	XP_011526511.1:p.Leu212=
XR_936204.1:n.1483G>T
XM_005259617.3:c.858G>T	XP_005259674.1:p.Leu286=
XM_011528209.2:c.636G>T	XP_011526511.1:p.Leu212=
XR_001753738.2:n.1483G>T
XR_001753739.1:n.1483G>T
XR_001753740.2:n.1483G>T
NM_000455.5:c.858G>T MANE Select	NP_000446.1:p.Leu286=