Canonical Allele Identifier: CA2582597003

Gene: STK11

Linked Data

• gnomAD v4: 19-1226205-CAGGT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1226206_1226209del , CM000681.2:g.1226206_1226209del	GRCh38
NC_000019.9:g.1226205_1226208del , CM000681.1:g.1226205_1226208del	GRCh37
NC_000019.8:g.1177205_1177208del	NCBI36
NG_007460.2:g.41800_41803del , LRG_319:g.41800_41803del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.*2462_*2465del	ENSP00000490268.2:n.*2462_*2465del
ENST00000585748.3:c.737-248_737-245del	ENSP00000477641.2:n.737-248_737-245del
ENST00000585851.2:c.935-248_935-245del	ENSP00000467912.2:n.935-248_935-245del
ENST00000326873.12:c.1109-248_1109-245del MANE Select	ENSP00000324856.6:n.1109-248_1109-245del
ENST00000326873.11:c.1109-248_1109-245del	ENSP00000324856.6:n.1109-248_1109-245del
ENST00000585465.2:n.2594_2597del
ENST00000586243.5:c.1109-248_1109-245del	ENSP00000467240.2:n.1109-248_1109-245del
ENST00000589152.5:n.1807-248_1807-245del
NM_000455.4:c.1109-248_1109-245del , LRG_319t1:c.1109-248_1109-245del	NP_000446.1:n.1109-248_1109-245del
XM_005259617.1:c.1109-253_1109-250del	XP_005259674.1:n.1109-253_1109-250del
XM_011528209.1:c.887-253_887-250del	XP_011526511.1:n.887-253_887-250del
XM_005259617.3:c.1109-253_1109-250del	XP_005259674.1:n.1109-253_1109-250del
XM_011528209.2:c.887-253_887-250del	XP_011526511.1:n.887-253_887-250del
XR_001753738.2:n.1915-248_1915-245del
XR_001753740.2:n.1885-248_1885-245del
NM_000455.5:c.1109-248_1109-245del MANE Select	NP_000446.1:n.1109-248_1109-245del