Canonical Allele Identifier: CA2582591136

Gene: STK11

Linked Data

• gnomAD v4: 19-1206796-CCT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1206797_1206798del , CM000681.2:g.1206797_1206798del	GRCh38
NC_000019.9:g.1206796_1206797del , CM000681.1:g.1206796_1206797del	GRCh37
NC_000019.8:g.1157796_1157797del	NCBI36
NG_007460.2:g.22391_22392del , LRG_319:g.22391_22392del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.-117_-116del	ENSP00000490268.2:n.-117_-116del
ENST00000585748.3:c.-82-11620_-82-11619del	ENSP00000477641.2:n.-82-11620_-82-11619del
ENST00000326873.12:c.-117_-116del MANE Select	ENSP00000324856.6:n.-117_-116del
ENST00000652231.1:c.-117_-116del	ENSP00000498804.1:n.-117_-116del
ENST00000326873.11:c.-117_-116del	ENSP00000324856.6:n.-117_-116del
ENST00000585748.2:c.-82-11620_-82-11619del	ENSP00000477641.1:n.-82-11620_-82-11619del
ENST00000586243.5:c.-117_-116del	ENSP00000467240.2:n.-117_-116del
NM_000455.4:c.-117_-116del , LRG_319t1:c.-117_-116del	NP_000446.1:n.-117_-116del
XM_005259617.1:c.-117_-116del	XP_005259674.1:n.-117_-116del
XM_005259618.3:c.-117_-116del	XP_005259675.1:n.-117_-116del
XM_011528209.1:c.-470_-469del	XP_011526511.1:n.-470_-469del
XR_936204.1:n.509_510del
XM_005259617.3:c.-117_-116del	XP_005259674.1:n.-117_-116del
XM_011528209.2:c.-470_-469del	XP_011526511.1:n.-470_-469del
XR_001753738.2:n.509_510del
XR_001753739.1:n.509_510del
XR_001753740.2:n.509_510del
NM_000455.5:c.-117_-116del MANE Select	NP_000446.1:n.-117_-116del