Canonical Allele Identifier: CA402954272

Gene: STK11

Linked Data

• MyVariant Identifiers: chr19:g.1226635A>T (hg19) ; chr19:g.1226636A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1226636A>T , CM000681.2:g.1226636A>T	GRCh38
NC_000019.9:g.1226635A>T , CM000681.1:g.1226635A>T	GRCh37
NC_000019.8:g.1177635A>T	NCBI36
NG_007460.2:g.42230A>T , LRG_319:g.42230A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000585465.3:c.*2892A>T	ENSP00000490268.2:n.*2892A>T
ENST00000585748.3:c.919A>T	ENSP00000477641.2:p.Lys307Ter
ENST00000585851.2:c.1117A>T	ENSP00000467912.2:p.Lys373Ter
ENST00000326873.12:c.1291A>T MANE Select	ENSP00000324856.6:p.Lys431Ter
ENST00000326873.11:c.1291A>T	ENSP00000324856.6:p.Lys431Ter
ENST00000585465.2:n.3024A>T
ENST00000586243.5:c.1288A>T	ENSP00000467240.2:p.Lys430Ter
ENST00000589152.5:n.1989A>T
NM_000455.4:c.1291A>T , LRG_319t1:c.1291A>T	NP_000446.1:p.Lys431Ter
XM_005259617.1:c.1286A>T	XP_005259674.1:p.Gln429Leu
XM_011528209.1:c.1064A>T	XP_011526511.1:p.Gln355Leu
XM_005259617.3:c.1286A>T	XP_005259674.1:p.Gln429Leu
XM_011528209.2:c.1064A>T	XP_011526511.1:p.Gln355Leu
XR_001753738.2:n.2097A>T
XR_001753740.2:n.2067A>T
NM_000455.5:c.1291A>T MANE Select	NP_000446.1:p.Lys431Ter