Canonical Allele Identifier: CA402953414

Gene: STK11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1226501C>T , CM000681.2:g.1226501C>T	GRCh38
NC_000019.9:g.1226500C>T , CM000681.1:g.1226500C>T	GRCh37
NC_000019.8:g.1177500C>T	NCBI36
NG_007460.2:g.42095C>T , LRG_319:g.42095C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_000455.5:c.1156C>T MANE Select	NP_000446.1:p.Leu386Phe
ENST00000326873.12:c.1156C>T MANE Select	ENSP00000324856.6:p.Leu386Phe
NM_000455.4:c.1156C>T , LRG_319t1:c.1156C>T	NP_000446.1:p.Leu386Phe
ENST00000326873.11:c.1156C>T	ENSP00000324856.6:p.Leu386Phe
ENST00000585465.2:n.2889C>T
ENST00000585465.3:c.*2757C>T	ENSP00000490268.2:n.*2757C>T
ENST00000585748.3:c.784C>T	ENSP00000477641.2:p.Leu262Phe
ENST00000585851.2:c.982C>T	ENSP00000467912.2:p.Leu328Phe
ENST00000586243.5:c.1156C>T	ENSP00000467240.2:p.Leu386Phe
ENST00000589152.5:n.1854C>T
XM_005259617.1:c.1151C>T	XP_005259674.1:p.Pro384Leu
XM_005259617.3:c.1151C>T	XP_005259674.1:p.Pro384Leu
XM_011528209.1:c.929C>T	XP_011526511.1:p.Pro310Leu
XM_011528209.2:c.929C>T	XP_011526511.1:p.Pro310Leu
XR_001753738.2:n.1962C>T
XR_001753740.2:n.1932C>T