Canonical Allele Identifier: CA2582596953

Gene: STK11

Linked Data

• gnomAD v4: 19-1226148-CCTA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1226151_1226153del , CM000681.2:g.1226151_1226153del	GRCh38
NC_000019.9:g.1226150_1226152del , CM000681.1:g.1226150_1226152del	GRCh37
NC_000019.8:g.1177150_1177152del	NCBI36
NG_007460.2:g.41745_41747del , LRG_319:g.41745_41747del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.*2407_*2409del	ENSP00000490268.2:n.*2407_*2409del
ENST00000585748.3:c.737-303_737-301del	ENSP00000477641.2:n.737-303_737-301del
ENST00000585851.2:c.935-303_935-301del	ENSP00000467912.2:n.935-303_935-301del
ENST00000326873.12:c.1109-303_1109-301del MANE Select	ENSP00000324856.6:n.1109-303_1109-301del
ENST00000326873.11:c.1109-303_1109-301del	ENSP00000324856.6:n.1109-303_1109-301del
ENST00000585465.2:n.2539_2541del
ENST00000586243.5:c.1109-303_1109-301del	ENSP00000467240.2:n.1109-303_1109-301del
ENST00000589152.5:n.1807-303_1807-301del
NM_000455.4:c.1109-303_1109-301del , LRG_319t1:c.1109-303_1109-301del	NP_000446.1:n.1109-303_1109-301del
XM_005259617.1:c.1109-308_1109-306del	XP_005259674.1:n.1109-308_1109-306del
XM_011528209.1:c.887-308_887-306del	XP_011526511.1:n.887-308_887-306del
XM_005259617.3:c.1109-308_1109-306del	XP_005259674.1:n.1109-308_1109-306del
XM_011528209.2:c.887-308_887-306del	XP_011526511.1:n.887-308_887-306del
XR_001753738.2:n.1915-303_1915-301del
XR_001753740.2:n.1885-303_1885-301del
NM_000455.5:c.1109-303_1109-301del MANE Select	NP_000446.1:n.1109-303_1109-301del