Canonical Allele Identifier: CA2317589241

Gene: STK11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1219544_1219547delinsGTTT , CM000681.2:g.1219544_1219547delinsGTTT	GRCh38
NC_000019.9:g.1219543_1219546delinsGTTT , CM000681.1:g.1219543_1219546delinsGTTT	GRCh37
NC_000019.8:g.1170543_1170546delinsGTTT	NCBI36
NG_007460.2:g.35138_35141delinsGTTT , LRG_319:g.35138_35141delinsGTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.464+131_464+134delinsGTTT	ENSP00000490268.2:n.464+131_464+134delinsGTTT
ENST00000585748.3:c.92+131_92+134delinsGTTT	ENSP00000477641.2:n.92+131_92+134delinsGTTT
ENST00000585851.2:c.291-829_291-826delinsGTTT	ENSP00000467912.2:n.291-829_291-826delinsGTTT
ENST00000326873.12:c.464+131_464+134delinsGTTT MANE Select	ENSP00000324856.6:n.464+131_464+134delinsGTTT
ENST00000652231.1:c.464+131_464+134delinsGTTT	ENSP00000498804.1:n.464+131_464+134delinsGTTT
ENST00000326873.11:c.464+131_464+134delinsGTTT	ENSP00000324856.6:n.464+131_464+134delinsGTTT
ENST00000585851.1:c.291-829_291-826delinsGTTT	ENSP00000467912.1:n.291-829_291-826delinsGTTT
ENST00000586243.5:c.464+131_464+134delinsGTTT	ENSP00000467240.2:n.464+131_464+134delinsGTTT
ENST00000586358.5:n.287+131_287+134delinsGTTT
ENST00000589152.5:n.554+131_554+134delinsGTTT
NM_000455.4:c.464+131_464+134delinsGTTT , LRG_319t1:c.464+131_464+134delinsGTTT	NP_000446.1:n.464+131_464+134delinsGTTT
XM_005259617.1:c.464+131_464+134delinsGTTT	XP_005259674.1:n.464+131_464+134delinsGTTT
XM_005259618.3:c.464+131_464+134delinsGTTT	XP_005259675.1:n.464+131_464+134delinsGTTT
XM_011528209.1:c.242+131_242+134delinsGTTT	XP_011526511.1:n.242+131_242+134delinsGTTT
XR_936204.1:n.1089+131_1089+134delinsGTTT
XM_005259617.3:c.464+131_464+134delinsGTTT	XP_005259674.1:n.464+131_464+134delinsGTTT
XM_011528209.2:c.242+131_242+134delinsGTTT	XP_011526511.1:n.242+131_242+134delinsGTTT
XR_001753738.2:n.1089+131_1089+134delinsGTTT
XR_001753739.1:n.1089+131_1089+134delinsGTTT
XR_001753740.2:n.1089+131_1089+134delinsGTTT
NM_000455.5:c.464+131_464+134delinsGTTT MANE Select	NP_000446.1:n.464+131_464+134delinsGTTT