Canonical Allele Identifier: CA402953209

Gene: STK11

Linked Data

• gnomAD v4: 19-1226470-G-T
• MyVariant Identifiers: chr19:g.1226469G>T (hg19) ; chr19:g.1226470G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1226470G>T , CM000681.2:g.1226470G>T	GRCh38
NC_000019.9:g.1226469G>T , CM000681.1:g.1226469G>T	GRCh37
NC_000019.8:g.1177469G>T	NCBI36
NG_007460.2:g.42064G>T , LRG_319:g.42064G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.*2726G>T	ENSP00000490268.2:n.*2726G>T
ENST00000585748.3:c.753G>T	ENSP00000477641.2:p.Glu251Asp
ENST00000585851.2:c.951G>T	ENSP00000467912.2:p.Glu317Asp
ENST00000326873.12:c.1125G>T MANE Select	ENSP00000324856.6:p.Glu375Asp
ENST00000326873.11:c.1125G>T	ENSP00000324856.6:p.Glu375Asp
ENST00000585465.2:n.2858G>T
ENST00000586243.5:c.1125G>T	ENSP00000467240.2:p.Glu375Asp
ENST00000589152.5:n.1823G>T
NM_000455.4:c.1125G>T , LRG_319t1:c.1125G>T	NP_000446.1:p.Glu375Asp
XM_005259617.1:c.1120G>T	XP_005259674.1:p.Gly374Ter
XM_011528209.1:c.898G>T	XP_011526511.1:p.Gly300Ter
XM_005259617.3:c.1120G>T	XP_005259674.1:p.Gly374Ter
XM_011528209.2:c.898G>T	XP_011526511.1:p.Gly300Ter
XR_001753738.2:n.1931G>T
XR_001753740.2:n.1901G>T
NM_000455.5:c.1125G>T MANE Select	NP_000446.1:p.Glu375Asp