Canonical Allele Identifier: CA2582597000

Gene: STK11

Linked Data

• gnomAD v4: 19-1226545-GAGCACCAAATCC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1226548_1226559del , CM000681.2:g.1226548_1226559del	GRCh38
NC_000019.9:g.1226547_1226558del , CM000681.1:g.1226547_1226558del	GRCh37
NC_000019.8:g.1177547_1177558del	NCBI36
NG_007460.2:g.42142_42153del , LRG_319:g.42142_42153del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.*2804_*2815del	ENSP00000490268.2:n.*2804_*2815del
ENST00000585748.3:c.831_842del	ENSP00000477641.2:p.Ser277_Ser280del
ENST00000585851.2:c.1029_1040del	ENSP00000467912.2:p.Ser343_Ser346del
ENST00000326873.12:c.1203_1214del MANE Select	ENSP00000324856.6:p.Ser401_Ser404del
ENST00000326873.11:c.1203_1214del	ENSP00000324856.6:p.Ser401_Ser404del
ENST00000585465.2:n.2936_2947del
ENST00000586243.5:c.1203_1214del	ENSP00000467240.2:p.Ser401_Ser404del
ENST00000589152.5:n.1901_1912del
NM_000455.4:c.1203_1214del , LRG_319t1:c.1203_1214del	NP_000446.1:p.Ser401_Ser404del
XM_005259617.1:c.1198_1209del	XP_005259674.1:p.His400_Gln403del
XM_011528209.1:c.976_987del	XP_011526511.1:p.His326_Gln329del
XM_005259617.3:c.1198_1209del	XP_005259674.1:p.His400_Gln403del
XM_011528209.2:c.976_987del	XP_011526511.1:p.His326_Gln329del
XR_001753738.2:n.2009_2020del
XR_001753740.2:n.1979_1990del
NM_000455.5:c.1203_1214del MANE Select	NP_000446.1:p.Ser401_Ser404del