Canonical Allele Identifier: CA2813238352

Gene: STK11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1206773C>A , CM000681.2:g.1206773C>A	GRCh38
NC_000019.9:g.1206772C>A , CM000681.1:g.1206772C>A	GRCh37
NC_000019.8:g.1157772C>A	NCBI36
NG_007460.2:g.22367C>A , LRG_319:g.22367C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.-141C>A	ENSP00000490268.2:n.-141C>A
ENST00000585748.3:c.-82-11644C>A	ENSP00000477641.2:n.-82-11644C>A
ENST00000326873.12:c.-141C>A MANE Select	ENSP00000324856.6:n.-141C>A
ENST00000652231.1:c.-141C>A	ENSP00000498804.1:n.-141C>A
ENST00000326873.11:c.-141C>A	ENSP00000324856.6:n.-141C>A
ENST00000585748.2:c.-82-11644C>A	ENSP00000477641.1:n.-82-11644C>A
ENST00000586243.5:c.-141C>A	ENSP00000467240.2:n.-141C>A
NM_000455.4:c.-141C>A , LRG_319t1:c.-141C>A	NP_000446.1:n.-141C>A
XM_005259617.1:c.-141C>A	XP_005259674.1:n.-141C>A
XM_005259618.3:c.-141C>A	XP_005259675.1:n.-141C>A
XM_011528209.1:c.-494C>A	XP_011526511.1:n.-494C>A
XR_936204.1:n.485C>A
XM_005259617.3:c.-141C>A	XP_005259674.1:n.-141C>A
XM_011528209.2:c.-494C>A	XP_011526511.1:n.-494C>A
XR_001753738.2:n.485C>A
XR_001753739.1:n.485C>A
XR_001753740.2:n.485C>A
NM_000455.5:c.-141C>A MANE Select	NP_000446.1:n.-141C>A