Canonical Allele Identifier: CA402953593

Gene: STK11

Linked Data

• MyVariant Identifiers: chr19:g.1226528C>A (hg19) ; chr19:g.1226529C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1226529C>A , CM000681.2:g.1226529C>A	GRCh38
NC_000019.9:g.1226528C>A , CM000681.1:g.1226528C>A	GRCh37
NC_000019.8:g.1177528C>A	NCBI36
NG_007460.2:g.42123C>A , LRG_319:g.42123C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000585465.3:c.*2785C>A	ENSP00000490268.2:n.*2785C>A
ENST00000585748.3:c.812C>A	ENSP00000477641.2:p.Thr271Lys
ENST00000585851.2:c.1010C>A	ENSP00000467912.2:p.Thr337Lys
ENST00000326873.12:c.1184C>A MANE Select	ENSP00000324856.6:p.Thr395Lys
ENST00000326873.11:c.1184C>A	ENSP00000324856.6:p.Thr395Lys
ENST00000585465.2:n.2917C>A
ENST00000586243.5:c.1184C>A	ENSP00000467240.2:p.Thr395Lys
ENST00000589152.5:n.1882C>A
NM_000455.4:c.1184C>A , LRG_319t1:c.1184C>A	NP_000446.1:p.Thr395Lys
XM_005259617.1:c.1179C>A	XP_005259674.1:p.His393Gln
XM_011528209.1:c.957C>A	XP_011526511.1:p.His319Gln
XM_005259617.3:c.1179C>A	XP_005259674.1:p.His393Gln
XM_011528209.2:c.957C>A	XP_011526511.1:p.His319Gln
XR_001753738.2:n.1990C>A
XR_001753740.2:n.1960C>A
NM_000455.5:c.1184C>A MANE Select	NP_000446.1:p.Thr395Lys