Canonical Allele Identifier: CA2735577643

Gene: STK11

Linked Data

• dbSNP Id: rs2145424787

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1220525_1220534del , CM000681.2:g.1220525_1220534del	GRCh38
NC_000019.9:g.1220524_1220533del , CM000681.1:g.1220524_1220533del	GRCh37
NC_000019.8:g.1171524_1171533del	NCBI36
NG_007460.2:g.36119_36128del , LRG_319:g.36119_36128del

Transcript Alleles

HGVS	Amino-acid change
ENST00000585465.3:c.597+20_597+29del	ENSP00000490268.2:n.597+20_597+29del
ENST00000585748.3:c.225+20_225+29del	ENSP00000477641.2:n.225+20_225+29del
ENST00000585851.2:c.423+20_423+29del	ENSP00000467912.2:n.423+20_423+29del
ENST00000326873.12:c.597+20_597+29del MANE Select	ENSP00000324856.6:n.597+20_597+29del
ENST00000652231.1:c.597+20_597+29del	ENSP00000498804.1:n.597+20_597+29del
ENST00000326873.11:c.597+20_597+29del	ENSP00000324856.6:n.597+20_597+29del
ENST00000585851.1:c.423+20_423+29del	ENSP00000467912.1:n.423+20_423+29del
ENST00000586243.5:c.597+20_597+29del	ENSP00000467240.2:n.597+20_597+29del
ENST00000586358.5:n.440_449del
ENST00000589152.5:n.687+20_687+29del
ENST00000591133.2:n.513_522del
NM_000455.4:c.597+20_597+29del , LRG_319t1:c.597+20_597+29del	NP_000446.1:n.597+20_597+29del
XM_005259617.1:c.597+20_597+29del	XP_005259674.1:n.597+20_597+29del
XM_005259618.3:c.597+20_597+29del	XP_005259675.1:n.597+20_597+29del
XM_011528209.1:c.375+20_375+29del	XP_011526511.1:n.375+20_375+29del
XR_936204.1:n.1222+20_1222+29del
XM_005259617.3:c.597+20_597+29del	XP_005259674.1:n.597+20_597+29del
XM_011528209.2:c.375+20_375+29del	XP_011526511.1:n.375+20_375+29del
XR_001753738.2:n.1222+20_1222+29del
XR_001753739.1:n.1222+20_1222+29del
XR_001753740.2:n.1222+20_1222+29del
NM_000455.5:c.597+20_597+29del MANE Select	NP_000446.1:n.597+20_597+29del