Canonical Allele Identifier: CA2317593654

Gene: STK11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1226467_1226470delinsAGAG , CM000681.2:g.1226467_1226470delinsAGAG	GRCh38
NC_000019.9:g.1226466_1226469delinsAGAG , CM000681.1:g.1226466_1226469delinsAGAG	GRCh37
NC_000019.8:g.1177466_1177469delinsAGAG	NCBI36
NG_007460.2:g.42061_42064delinsAGAG , LRG_319:g.42061_42064delinsAGAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.*2723_*2726delinsAGAG	ENSP00000490268.2:n.*2723_*2726delinsAGAG
ENST00000585748.3:c.750_753delinsAGAG	ENSP00000477641.2:p.Glu250=
ENST00000585851.2:c.948_951delinsAGAG	ENSP00000467912.2:p.Glu316=
ENST00000326873.12:c.1122_1125delinsAGAG MANE Select	ENSP00000324856.6:p.Glu374=
ENST00000326873.11:c.1122_1125delinsAGAG	ENSP00000324856.6:p.Glu374=
ENST00000585465.2:n.2855_2858delinsAGAG
ENST00000586243.5:c.1122_1125delinsAGAG	ENSP00000467240.2:p.Glu374=
ENST00000589152.5:n.1820_1823delinsAGAG
NM_000455.4:c.1122_1125delinsAGAG , LRG_319t1:c.1122_1125delinsAGAG	NP_000446.1:p.Glu374=
XM_005259617.1:c.1117_1120delinsAGAG	XP_005259674.1:p.Arg373=
XM_011528209.1:c.895_898delinsAGAG	XP_011526511.1:p.Arg299=
XM_005259617.3:c.1117_1120delinsAGAG	XP_005259674.1:p.Arg373=
XM_011528209.2:c.895_898delinsAGAG	XP_011526511.1:p.Arg299=
XR_001753738.2:n.1928_1931delinsAGAG
XR_001753740.2:n.1898_1901delinsAGAG
NM_000455.5:c.1122_1125delinsAGAG MANE Select	NP_000446.1:p.Glu374=