Canonical Allele Identifier: CA2695227914

Gene: STK11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1220521_1220538delinsTG , CM000681.2:g.1220521_1220538delinsTG	GRCh38
NC_000019.9:g.1220520_1220537delinsTG , CM000681.1:g.1220520_1220537delinsTG	GRCh37
NC_000019.8:g.1171520_1171537delinsTG	NCBI36
NG_007460.2:g.36115_36132delinsTG , LRG_319:g.36115_36132delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.597+16_597+33delinsTG	ENSP00000490268.2:n.597+16_597+33delinsTG
ENST00000585748.3:c.225+16_225+33delinsTG	ENSP00000477641.2:n.225+16_225+33delinsTG
ENST00000585851.2:c.423+16_423+33delinsTG	ENSP00000467912.2:n.423+16_423+33delinsTG
ENST00000326873.12:c.597+16_597+33delinsTG MANE Select	ENSP00000324856.6:n.597+16_597+33delinsTG
ENST00000652231.1:c.597+16_597+33delinsTG	ENSP00000498804.1:n.597+16_597+33delinsTG
ENST00000326873.11:c.597+16_597+33delinsTG	ENSP00000324856.6:n.597+16_597+33delinsTG
ENST00000585851.1:c.423+16_423+33delinsTG	ENSP00000467912.1:n.423+16_423+33delinsTG
ENST00000586243.5:c.597+16_597+33delinsTG	ENSP00000467240.2:n.597+16_597+33delinsTG
ENST00000586358.5:n.436_453delinsTG
ENST00000589152.5:n.687+16_687+33delinsTG
ENST00000591133.2:n.509_526delinsTG
NM_000455.4:c.597+16_597+33delinsTG , LRG_319t1:c.597+16_597+33delinsTG	NP_000446.1:n.597+16_597+33delinsTG
XM_005259617.1:c.597+16_597+33delinsTG	XP_005259674.1:n.597+16_597+33delinsTG
XM_005259618.3:c.597+16_597+33delinsTG	XP_005259675.1:n.597+16_597+33delinsTG
XM_011528209.1:c.375+16_375+33delinsTG	XP_011526511.1:n.375+16_375+33delinsTG
XR_936204.1:n.1222+16_1222+33delinsTG
XM_005259617.3:c.597+16_597+33delinsTG	XP_005259674.1:n.597+16_597+33delinsTG
XM_011528209.2:c.375+16_375+33delinsTG	XP_011526511.1:n.375+16_375+33delinsTG
XR_001753738.2:n.1222+16_1222+33delinsTG
XR_001753739.1:n.1222+16_1222+33delinsTG
XR_001753740.2:n.1222+16_1222+33delinsTG
NM_000455.5:c.597+16_597+33delinsTG MANE Select	NP_000446.1:n.597+16_597+33delinsTG