Canonical Allele Identifier: CA2813238360

Gene: STK11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1206814_1206815insTTTTTTTAAA , CM000681.2:g.1206814_1206815insTTTTTTTAAA	GRCh38
NC_000019.9:g.1206813_1206814insTTTTTTTAAA , CM000681.1:g.1206813_1206814insTTTTTTTAAA	GRCh37
NC_000019.8:g.1157813_1157814insTTTTTTTAAA	NCBI36
NG_007460.2:g.22408_22409insTTTTTTTAAA , LRG_319:g.22408_22409insTTTTTTTAAA

Transcript Alleles

HGVS	Amino-acid change
ENST00000585465.3:c.-100_-99insTTTTTTTAAA	ENSP00000490268.2:n.-100_-99insTTTTTTTAAA
ENST00000585748.3:c.-82-11603_-82-11602insTTTTTTTAAA	ENSP00000477641.2:n.-82-11603_-82-11602insTTTTTTTAAA
ENST00000326873.12:c.-100_-99insTTTTTTTAAA MANE Select	ENSP00000324856.6:n.-100_-99insTTTTTTTAAA
ENST00000652231.1:c.-100_-99insTTTTTTTAAA	ENSP00000498804.1:n.-100_-99insTTTTTTTAAA
ENST00000326873.11:c.-100_-99insTTTTTTTAAA	ENSP00000324856.6:n.-100_-99insTTTTTTTAAA
ENST00000585748.2:c.-82-11603_-82-11602insTTTTTTTAAA	ENSP00000477641.1:n.-82-11603_-82-11602insTTTTTTTAAA
ENST00000586243.5:c.-100_-99insTTTTTTTAAA	ENSP00000467240.2:n.-100_-99insTTTTTTTAAA
NM_000455.4:c.-100_-99insTTTTTTTAAA , LRG_319t1:c.-100_-99insTTTTTTTAAA	NP_000446.1:n.-100_-99insTTTTTTTAAA
XM_005259617.1:c.-100_-99insTTTTTTTAAA	XP_005259674.1:n.-100_-99insTTTTTTTAAA
XM_005259618.3:c.-100_-99insTTTTTTTAAA	XP_005259675.1:n.-100_-99insTTTTTTTAAA
XM_011528209.1:c.-453_-452insTTTTTTTAAA	XP_011526511.1:n.-453_-452insTTTTTTTAAA
XR_936204.1:n.526_527insTTTTTTTAAA
XM_005259617.3:c.-100_-99insTTTTTTTAAA	XP_005259674.1:n.-100_-99insTTTTTTTAAA
XM_011528209.2:c.-453_-452insTTTTTTTAAA	XP_011526511.1:n.-453_-452insTTTTTTTAAA
XR_001753738.2:n.526_527insTTTTTTTAAA
XR_001753739.1:n.526_527insTTTTTTTAAA
XR_001753740.2:n.526_527insTTTTTTTAAA
NM_000455.5:c.-100_-99insTTTTTTTAAA MANE Select	NP_000446.1:n.-100_-99insTTTTTTTAAA