Canonical Allele Identifier: CA022164

Gene: STK11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1223080C>T , CM000681.2:g.1223080C>T	GRCh38
NC_000019.9:g.1223079C>T , CM000681.1:g.1223079C>T	GRCh37
NC_000019.8:g.1174079C>T	NCBI36
NG_007460.2:g.38674C>T , LRG_319:g.38674C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_000455.5:c.1016C>T MANE Select	NP_000446.1:p.Pro339Leu
ENST00000326873.12:c.1016C>T MANE Select	ENSP00000324856.6:p.Pro339Leu
NM_000455.4:c.1016C>T , LRG_319t1:c.1016C>T	NP_000446.1:p.Pro339Leu
ENST00000326873.11:c.1016C>T	ENSP00000324856.6:p.Pro339Leu
ENST00000585465.3:c.1016C>T	ENSP00000490268.2:p.Pro339Leu
ENST00000585748.3:c.644C>T	ENSP00000477641.2:p.Pro215Leu
ENST00000585851.2:c.842C>T	ENSP00000467912.2:p.Pro281Leu
ENST00000586243.5:c.1016C>T	ENSP00000467240.2:p.Pro339Leu
ENST00000589152.5:n.1714C>T
ENST00000591133.2:n.987C>T
ENST00000652231.1:c.1016C>T	ENSP00000498804.1:p.Pro339Leu
XM_005259617.1:c.1016C>T	XP_005259674.1:p.Pro339Leu
XM_005259617.3:c.1016C>T	XP_005259674.1:p.Pro339Leu
XM_005259618.3:c.1016C>T	XP_005259675.1:p.Pro339Leu
XM_011528209.1:c.794C>T	XP_011526511.1:p.Pro265Leu
XM_011528209.2:c.794C>T	XP_011526511.1:p.Pro265Leu
XR_001753738.2:n.1822C>T
XR_001753739.1:n.1822C>T
XR_001753740.2:n.1792C>T
XR_936204.1:n.1792C>T