Canonical Allele Identifier: CA402953359

Gene: STK11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1226491G>T , CM000681.2:g.1226491G>T	GRCh38
NC_000019.9:g.1226490G>T , CM000681.1:g.1226490G>T	GRCh37
NC_000019.8:g.1177490G>T	NCBI36
NG_007460.2:g.42085G>T , LRG_319:g.42085G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_000455.5:c.1146G>T MANE Select	NP_000446.1:p.Gln382His
ENST00000326873.12:c.1146G>T MANE Select	ENSP00000324856.6:p.Gln382His
NM_000455.4:c.1146G>T , LRG_319t1:c.1146G>T	NP_000446.1:p.Gln382His
ENST00000326873.11:c.1146G>T	ENSP00000324856.6:p.Gln382His
ENST00000585465.2:n.2879G>T
ENST00000585465.3:c.*2747G>T	ENSP00000490268.2:n.*2747G>T
ENST00000585748.3:c.774G>T	ENSP00000477641.2:p.Gln258His
ENST00000585851.2:c.972G>T	ENSP00000467912.2:p.Gln324His
ENST00000586243.5:c.1146G>T	ENSP00000467240.2:p.Gln382His
ENST00000589152.5:n.1844G>T
XM_005259617.1:c.1141G>T	XP_005259674.1:p.Ala381Ser
XM_005259617.3:c.1141G>T	XP_005259674.1:p.Ala381Ser
XM_011528209.1:c.919G>T	XP_011526511.1:p.Ala307Ser
XM_011528209.2:c.919G>T	XP_011526511.1:p.Ala307Ser
XR_001753738.2:n.1952G>T
XR_001753740.2:n.1922G>T