Canonical Allele Identifier: CA402953888

Gene: STK11

Linked Data

• dbSNP Id: rs2145436338
• MyVariant Identifiers: chr19:g.1226576C>G (hg19) ; chr19:g.1226577C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1226577C>G , CM000681.2:g.1226577C>G	GRCh38
NC_000019.9:g.1226576C>G , CM000681.1:g.1226576C>G	GRCh37
NC_000019.8:g.1177576C>G	NCBI36
NG_007460.2:g.42171C>G , LRG_319:g.42171C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.*2833C>G	ENSP00000490268.2:n.*2833C>G
ENST00000585748.3:c.860C>G	ENSP00000477641.2:p.Pro287Arg
ENST00000585851.2:c.1058C>G	ENSP00000467912.2:p.Pro353Arg
ENST00000326873.12:c.1232C>G MANE Select	ENSP00000324856.6:p.Pro411Arg
ENST00000326873.11:c.1232C>G	ENSP00000324856.6:p.Pro411Arg
ENST00000585465.2:n.2965C>G
ENST00000586243.5:c.1231C>G	ENSP00000467240.2:p.Pro411Ala
ENST00000589152.5:n.1930C>G
NM_000455.4:c.1232C>G , LRG_319t1:c.1232C>G	NP_000446.1:p.Pro411Arg
XM_005259617.1:c.1227C>G	XP_005259674.1:p.Pro409=
XM_011528209.1:c.1005C>G	XP_011526511.1:p.Pro335=
XM_005259617.3:c.1227C>G	XP_005259674.1:p.Pro409=
XM_011528209.2:c.1005C>G	XP_011526511.1:p.Pro335=
XR_001753738.2:n.2038C>G
XR_001753740.2:n.2008C>G
NM_000455.5:c.1232C>G MANE Select	NP_000446.1:p.Pro411Arg