Canonical Allele Identifier: CA504708438

Gene: STK11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1226500C>G , CM000681.2:g.1226500C>G	GRCh38
NC_000019.9:g.1226499C>G , CM000681.1:g.1226499C>G	GRCh37
NC_000019.8:g.1177499C>G	NCBI36
NG_007460.2:g.42094C>G , LRG_319:g.42094C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_000455.5:c.1155C>G MANE Select	NP_000446.1:p.Gly385=
ENST00000326873.12:c.1155C>G MANE Select	ENSP00000324856.6:p.Gly385=
NM_000455.4:c.1155C>G , LRG_319t1:c.1155C>G	NP_000446.1:p.Gly385=
ENST00000326873.11:c.1155C>G	ENSP00000324856.6:p.Gly385=
ENST00000585465.2:n.2888C>G
ENST00000585465.3:c.*2756C>G	ENSP00000490268.2:n.*2756C>G
ENST00000585748.3:c.783C>G	ENSP00000477641.2:p.Gly261=
ENST00000585851.2:c.981C>G	ENSP00000467912.2:p.Gly327=
ENST00000586243.5:c.1155C>G	ENSP00000467240.2:p.Gly385=
ENST00000589152.5:n.1853C>G
XM_005259617.1:c.1150C>G	XP_005259674.1:p.Pro384Ala
XM_005259617.3:c.1150C>G	XP_005259674.1:p.Pro384Ala
XM_011528209.1:c.928C>G	XP_011526511.1:p.Pro310Ala
XM_011528209.2:c.928C>G	XP_011526511.1:p.Pro310Ala
XR_001753738.2:n.1961C>G
XR_001753740.2:n.1931C>G