Canonical Allele Identifier: CA2317589968

Gene: STK11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1220706_1220707delinsTG , CM000681.2:g.1220706_1220707delinsTG	GRCh38
NC_000019.9:g.1220705_1220706delinsTG , CM000681.1:g.1220705_1220706delinsTG	GRCh37
NC_000019.8:g.1171705_1171706delinsTG	NCBI36
NG_007460.2:g.36300_36301delinsTG , LRG_319:g.36300_36301delinsTG

Transcript Alleles

HGVS	Amino-acid change
ENST00000585465.3:c.723_724delinsTG	ENSP00000490268.2:p.Ala241=
ENST00000585748.3:c.351_352delinsTG	ENSP00000477641.2:p.Ala117=
ENST00000585851.2:c.549_550delinsTG	ENSP00000467912.2:p.Ala183=
ENST00000326873.12:c.723_724delinsTG MANE Select	ENSP00000324856.6:p.Ala241=
ENST00000652231.1:c.723_724delinsTG	ENSP00000498804.1:p.Ala241=
ENST00000326873.11:c.723_724delinsTG	ENSP00000324856.6:p.Ala241=
ENST00000586243.5:c.723_724delinsTG	ENSP00000467240.2:p.Ala241=
ENST00000586358.5:n.621_622delinsTG
ENST00000589152.5:n.813_814delinsTG
ENST00000591133.2:n.694_695delinsTG
NM_000455.4:c.723_724delinsTG , LRG_319t1:c.723_724delinsTG	NP_000446.1:p.Ala241=
XM_005259617.1:c.723_724delinsTG	XP_005259674.1:p.Ala241=
XM_005259618.3:c.723_724delinsTG	XP_005259675.1:p.Ala241=
XM_011528209.1:c.501_502delinsTG	XP_011526511.1:p.Ala167=
XR_936204.1:n.1348_1349delinsTG
XM_005259617.3:c.723_724delinsTG	XP_005259674.1:p.Ala241=
XM_011528209.2:c.501_502delinsTG	XP_011526511.1:p.Ala167=
XR_001753738.2:n.1348_1349delinsTG
XR_001753739.1:n.1348_1349delinsTG
XR_001753740.2:n.1348_1349delinsTG
NM_000455.5:c.723_724delinsTG MANE Select	NP_000446.1:p.Ala241=