Canonical Allele Identifier: CA2735355489

Gene: STK11

Linked Data

• dbSNP Id: rs1064794167

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1226472_1226474dup , CM000681.2:g.1226472_1226474dup	GRCh38
NC_000019.9:g.1226471_1226473dup , CM000681.1:g.1226471_1226473dup	GRCh37
NC_000019.8:g.1177471_1177473dup	NCBI36
NG_007460.2:g.42066_42068dup , LRG_319:g.42066_42068dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.*2728_*2730dup	ENSP00000490268.2:n.*2728_*2730dup
ENST00000585748.3:c.755_757dup	ENSP00000477641.2:p.Glu252_Ala253insGlu
ENST00000585851.2:c.953_955dup	ENSP00000467912.2:p.Glu318_Ala319insGlu
ENST00000326873.12:c.1127_1129dup MANE Select	ENSP00000324856.6:p.Glu376_Ala377insGlu
ENST00000326873.11:c.1127_1129dup	ENSP00000324856.6:p.Glu376_Ala377insGlu
ENST00000585465.2:n.2860_2862dup
ENST00000586243.5:c.1127_1129dup	ENSP00000467240.2:p.Glu376_Ala377insGlu
ENST00000589152.5:n.1825_1827dup
NM_000455.4:c.1127_1129dup , LRG_319t1:c.1127_1129dup	NP_000446.1:p.Glu376_Ala377insGlu
XM_005259617.1:c.1122_1124dup	XP_005259674.1:p.Gly375_Gln376insGly
XM_011528209.1:c.900_902dup	XP_011526511.1:p.Gly301_Gln302insGly
XM_005259617.3:c.1122_1124dup	XP_005259674.1:p.Gly375_Gln376insGly
XM_011528209.2:c.900_902dup	XP_011526511.1:p.Gly301_Gln302insGly
XR_001753738.2:n.1933_1935dup
XR_001753740.2:n.1903_1905dup
NM_000455.5:c.1127_1129dup MANE Select	NP_000446.1:p.Glu376_Ala377insGlu