Canonical Allele Identifier: CA2317593716

Gene: STK11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1226537_1226538delinsGC , CM000681.2:g.1226537_1226538delinsGC	GRCh38
NC_000019.9:g.1226536_1226537delinsGC , CM000681.1:g.1226536_1226537delinsGC	GRCh37
NC_000019.8:g.1177536_1177537delinsGC	NCBI36
NG_007460.2:g.42131_42132delinsGC , LRG_319:g.42131_42132delinsGC

Transcript Alleles

HGVS	Amino-acid change
ENST00000585465.3:c.*2793_*2794delinsGC	ENSP00000490268.2:n.*2793_*2794delinsGC
ENST00000585748.3:c.820_821delinsGC	ENSP00000477641.2:p.Ala274=
ENST00000585851.2:c.1018_1019delinsGC	ENSP00000467912.2:p.Ala340=
ENST00000326873.12:c.1192_1193delinsGC MANE Select	ENSP00000324856.6:p.Ala398=
ENST00000326873.11:c.1192_1193delinsGC	ENSP00000324856.6:p.Ala398=
ENST00000585465.2:n.2925_2926delinsGC
ENST00000586243.5:c.1192_1193delinsGC	ENSP00000467240.2:p.Ala398=
ENST00000589152.5:n.1890_1891delinsGC
NM_000455.4:c.1192_1193delinsGC , LRG_319t1:c.1192_1193delinsGC	NP_000446.1:p.Ala398=
XM_005259617.1:c.1187_1188delinsGC	XP_005259674.1:p.Gly396=
XM_011528209.1:c.965_966delinsGC	XP_011526511.1:p.Gly322=
XM_005259617.3:c.1187_1188delinsGC	XP_005259674.1:p.Gly396=
XM_011528209.2:c.965_966delinsGC	XP_011526511.1:p.Gly322=
XR_001753738.2:n.1998_1999delinsGC
XR_001753740.2:n.1968_1969delinsGC
NM_000455.5:c.1192_1193delinsGC MANE Select	NP_000446.1:p.Ala398=