Canonical Allele Identifier: CA402951335

Gene: STK11

Linked Data

• dbSNP Id: rs2145428889
• gnomAD v4: 19-1222005-A-T
• MyVariant Identifiers: chr19:g.1222004A>T (hg19) ; chr19:g.1222005A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1222005A>T , CM000681.2:g.1222005A>T	GRCh38
NC_000019.9:g.1222004A>T , CM000681.1:g.1222004A>T	GRCh37
NC_000019.8:g.1173004A>T	NCBI36
NG_007460.2:g.37599A>T , LRG_319:g.37599A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000585465.3:c.919A>T	ENSP00000490268.2:p.Ser307Cys
ENST00000585748.3:c.547A>T	ENSP00000477641.2:p.Ser183Cys
ENST00000585851.2:c.745A>T	ENSP00000467912.2:p.Ser249Cys
ENST00000326873.12:c.919A>T MANE Select	ENSP00000324856.6:p.Ser307Cys
ENST00000652231.1:c.919A>T	ENSP00000498804.1:p.Ser307Cys
ENST00000326873.11:c.919A>T	ENSP00000324856.6:p.Ser307Cys
ENST00000586243.5:c.919A>T	ENSP00000467240.2:p.Ser307Cys
ENST00000589152.5:n.1617A>T
ENST00000591133.2:n.890A>T
NM_000455.4:c.919A>T , LRG_319t1:c.919A>T	NP_000446.1:p.Ser307Cys
XM_005259617.1:c.919A>T	XP_005259674.1:p.Ser307Cys
XM_005259618.3:c.919A>T	XP_005259675.1:p.Ser307Cys
XM_011528209.1:c.697A>T	XP_011526511.1:p.Ser233Cys
XR_936204.1:n.1695A>T
XM_005259617.3:c.919A>T	XP_005259674.1:p.Ser307Cys
XM_011528209.2:c.697A>T	XP_011526511.1:p.Ser233Cys
XR_001753738.2:n.1725A>T
XR_001753739.1:n.1725A>T
XR_001753740.2:n.1695A>T
NM_000455.5:c.919A>T MANE Select	NP_000446.1:p.Ser307Cys