Canonical Allele Identifier: CA2317589842

Gene: STK11

Linked Data

• dbSNP Id: rs2080775423

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1220541dup , CM000681.2:g.1220541dup	GRCh38
NC_000019.9:g.1220540dup , CM000681.1:g.1220540dup	GRCh37
NC_000019.8:g.1171540dup	NCBI36
NG_007460.2:g.36135dup , LRG_319:g.36135dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.597+36dup	ENSP00000490268.2:n.597+36dup
ENST00000585748.3:c.225+36dup	ENSP00000477641.2:n.225+36dup
ENST00000585851.2:c.423+36dup	ENSP00000467912.2:n.423+36dup
ENST00000326873.12:c.597+36dup MANE Select	ENSP00000324856.6:n.597+36dup
ENST00000652231.1:c.597+36dup	ENSP00000498804.1:n.597+36dup
ENST00000326873.11:c.597+36dup	ENSP00000324856.6:n.597+36dup
ENST00000585851.1:c.423+36dup	ENSP00000467912.1:n.423+36dup
ENST00000586243.5:c.597+36dup	ENSP00000467240.2:n.597+36dup
ENST00000586358.5:n.456dup
ENST00000589152.5:n.687+36dup
ENST00000591133.2:n.529dup
NM_000455.4:c.597+36dup , LRG_319t1:c.597+36dup	NP_000446.1:n.597+36dup
XM_005259617.1:c.597+36dup	XP_005259674.1:n.597+36dup
XM_005259618.3:c.597+36dup	XP_005259675.1:n.597+36dup
XM_011528209.1:c.375+36dup	XP_011526511.1:n.375+36dup
XR_936204.1:n.1222+36dup
XM_005259617.3:c.597+36dup	XP_005259674.1:n.597+36dup
XM_011528209.2:c.375+36dup	XP_011526511.1:n.375+36dup
XR_001753738.2:n.1222+36dup
XR_001753739.1:n.1222+36dup
XR_001753740.2:n.1222+36dup
NM_000455.5:c.597+36dup MANE Select	NP_000446.1:n.597+36dup