Canonical Allele Identifier: CA402953820

Gene: STK11

Linked Data

• MyVariant Identifiers: chr19:g.1226566G>T (hg19) ; chr19:g.1226567G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1226567G>T , CM000681.2:g.1226567G>T	GRCh38
NC_000019.9:g.1226566G>T , CM000681.1:g.1226566G>T	GRCh37
NC_000019.8:g.1177566G>T	NCBI36
NG_007460.2:g.42161G>T , LRG_319:g.42161G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.*2823G>T	ENSP00000490268.2:n.*2823G>T
ENST00000585748.3:c.850G>T	ENSP00000477641.2:p.Gly284Cys
ENST00000585851.2:c.1048G>T	ENSP00000467912.2:p.Gly350Cys
ENST00000326873.12:c.1222G>T MANE Select	ENSP00000324856.6:p.Gly408Cys
ENST00000326873.11:c.1222G>T	ENSP00000324856.6:p.Gly408Cys
ENST00000585465.2:n.2955G>T
ENST00000586243.5:c.1222-1G>T	ENSP00000467240.2:n.1222-1G>T
ENST00000589152.5:n.1920G>T
NM_000455.4:c.1222G>T , LRG_319t1:c.1222G>T	NP_000446.1:p.Gly408Cys
XM_005259617.1:c.1217G>T	XP_005259674.1:p.Gly406Val
XM_011528209.1:c.995G>T	XP_011526511.1:p.Gly332Val
XM_005259617.3:c.1217G>T	XP_005259674.1:p.Gly406Val
XM_011528209.2:c.995G>T	XP_011526511.1:p.Gly332Val
XR_001753738.2:n.2028G>T
XR_001753740.2:n.1998G>T
NM_000455.5:c.1222G>T MANE Select	NP_000446.1:p.Gly408Cys