Canonical Allele Identifier: CA402950567

Gene: STK11

Linked Data

• MyVariant Identifiers: chr19:g.1221280G>T (hg19) ; chr19:g.1221281G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1221281G>T , CM000681.2:g.1221281G>T	GRCh38
NC_000019.9:g.1221280G>T , CM000681.1:g.1221280G>T	GRCh37
NC_000019.8:g.1172280G>T	NCBI36
NG_007460.2:g.36875G>T , LRG_319:g.36875G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.803G>T	ENSP00000490268.2:p.Gly268Val
ENST00000585748.3:c.431G>T	ENSP00000477641.2:p.Gly144Val
ENST00000585851.2:c.629G>T	ENSP00000467912.2:p.Gly210Val
ENST00000326873.12:c.803G>T MANE Select	ENSP00000324856.6:p.Gly268Val
ENST00000652231.1:c.803G>T	ENSP00000498804.1:p.Gly268Val
ENST00000326873.11:c.803G>T	ENSP00000324856.6:p.Gly268Val
ENST00000586243.5:c.803G>T	ENSP00000467240.2:p.Gly268Val
ENST00000586358.5:n.701G>T
ENST00000589152.5:n.893G>T
ENST00000591133.2:n.774G>T
NM_000455.4:c.803G>T , LRG_319t1:c.803G>T	NP_000446.1:p.Gly268Val
XM_005259617.1:c.803G>T	XP_005259674.1:p.Gly268Val
XM_005259618.3:c.803G>T	XP_005259675.1:p.Gly268Val
XM_011528209.1:c.581G>T	XP_011526511.1:p.Gly194Val
XR_936204.1:n.1428G>T
XM_005259617.3:c.803G>T	XP_005259674.1:p.Gly268Val
XM_011528209.2:c.581G>T	XP_011526511.1:p.Gly194Val
XR_001753738.2:n.1428G>T
XR_001753739.1:n.1428G>T
XR_001753740.2:n.1428G>T
NM_000455.5:c.803G>T MANE Select	NP_000446.1:p.Gly268Val