Canonical Allele Identifier: CA402953999

Gene: STK11

Linked Data

• dbSNP Id: rs1446554442
• MyVariant Identifiers: chr19:g.1226591A>T (hg19) ; chr19:g.1226592A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1226592A>T , CM000681.2:g.1226592A>T	GRCh38
NC_000019.9:g.1226591A>T , CM000681.1:g.1226591A>T	GRCh37
NC_000019.8:g.1177591A>T	NCBI36
NG_007460.2:g.42186A>T , LRG_319:g.42186A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.*2848A>T	ENSP00000490268.2:n.*2848A>T
ENST00000585748.3:c.875A>T	ENSP00000477641.2:p.Lys292Met
ENST00000585851.2:c.1073A>T	ENSP00000467912.2:p.Lys358Met
ENST00000326873.12:c.1247A>T MANE Select	ENSP00000324856.6:p.Lys416Met
ENST00000326873.11:c.1247A>T	ENSP00000324856.6:p.Lys416Met
ENST00000585465.2:n.2980A>T
ENST00000586243.5:c.1246A>T	ENSP00000467240.2:p.Arg416Trp
ENST00000589152.5:n.1945A>T
NM_000455.4:c.1247A>T , LRG_319t1:c.1247A>T	NP_000446.1:p.Lys416Met
XM_005259617.1:c.1242A>T	XP_005259674.1:p.Gln414His
XM_011528209.1:c.1020A>T	XP_011526511.1:p.Gln340His
XM_005259617.3:c.1242A>T	XP_005259674.1:p.Gln414His
XM_011528209.2:c.1020A>T	XP_011526511.1:p.Gln340His
XR_001753738.2:n.2053A>T
XR_001753740.2:n.2023A>T
NM_000455.5:c.1247A>T MANE Select	NP_000446.1:p.Lys416Met