Canonical Allele Identifier: CA304035606

Gene: STK11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1227908C>T , CM000681.2:g.1227908C>T	GRCh38
NC_000019.9:g.1227907C>T , CM000681.1:g.1227907C>T	GRCh37
NC_000019.8:g.1178907C>T	NCBI36
NG_007460.2:g.43502C>T , LRG_319:g.43502C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_000455.5:c.*332C>T MANE Select	NP_000446.1:n.*332C>T
ENST00000326873.12:c.*332C>T MANE Select	ENSP00000324856.6:n.*332C>T
NM_000455.4:c.*332C>T , LRG_319t1:c.*332C>T	NP_000446.1:n.*332C>T
ENST00000326873.11:c.*332C>T	ENSP00000324856.6:n.*332C>T
ENST00000585465.2:n.3367C>T
ENST00000585465.3:c.*3235C>T	ENSP00000490268.2:n.*3235C>T
ENST00000585748.3:c.*332C>T	ENSP00000477641.2:n.*332C>T
ENST00000585851.2:c.*332C>T	ENSP00000467912.2:n.*332C>T
ENST00000586243.5:c.*332C>T	ENSP00000467240.2:n.*332C>T
ENST00000589152.5:n.3261C>T
XM_005259617.1:c.1629C>T	XP_005259674.1:p.Ser543=
XM_005259617.3:c.1629C>T	XP_005259674.1:p.Ser543=
XM_011528209.1:c.1407C>T	XP_011526511.1:p.Ser469=
XM_011528209.2:c.1407C>T	XP_011526511.1:p.Ser469=
XR_001753738.2:n.2440C>T
XR_001753740.2:n.2410C>T