Canonical Allele Identifier: CA2317591442

Gene: STK11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1222992_1222993delinsCG , CM000681.2:g.1222992_1222993delinsCG	GRCh38
NC_000019.9:g.1222991_1222992delinsCG , CM000681.1:g.1222991_1222992delinsCG	GRCh37
NC_000019.8:g.1173991_1173992delinsCG	NCBI36
NG_007460.2:g.38586_38587delinsCG , LRG_319:g.38586_38587delinsCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.928_929delinsCG	ENSP00000490268.2:p.Arg310=
ENST00000585748.3:c.556_557delinsCG	ENSP00000477641.2:p.Arg186=
ENST00000585851.2:c.754_755delinsCG	ENSP00000467912.2:p.Arg252=
ENST00000326873.12:c.928_929delinsCG MANE Select	ENSP00000324856.6:p.Arg310=
ENST00000652231.1:c.928_929delinsCG	ENSP00000498804.1:p.Arg310=
ENST00000326873.11:c.928_929delinsCG	ENSP00000324856.6:p.Arg310=
ENST00000586243.5:c.928_929delinsCG	ENSP00000467240.2:p.Arg310=
ENST00000589152.5:n.1626_1627delinsCG
ENST00000591133.2:n.899_900delinsCG
NM_000455.4:c.928_929delinsCG , LRG_319t1:c.928_929delinsCG	NP_000446.1:p.Arg310=
XM_005259617.1:c.928_929delinsCG	XP_005259674.1:p.Arg310=
XM_005259618.3:c.928_929delinsCG	XP_005259675.1:p.Arg310=
XM_011528209.1:c.706_707delinsCG	XP_011526511.1:p.Arg236=
XR_936204.1:n.1704_1705delinsCG
XM_005259617.3:c.928_929delinsCG	XP_005259674.1:p.Arg310=
XM_011528209.2:c.706_707delinsCG	XP_011526511.1:p.Arg236=
XR_001753738.2:n.1734_1735delinsCG
XR_001753739.1:n.1734_1735delinsCG
XR_001753740.2:n.1704_1705delinsCG
NM_000455.5:c.928_929delinsCG MANE Select	NP_000446.1:p.Arg310=