Canonical Allele Identifier: CA2695227889

Gene: STK11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1220382_1220388del , CM000681.2:g.1220382_1220388del	GRCh38
NC_000019.9:g.1220381_1220387del , CM000681.1:g.1220381_1220387del	GRCh37
NC_000019.8:g.1171381_1171387del	NCBI36
NG_007460.2:g.35976_35982del , LRG_319:g.35976_35982del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.474_480del	ENSP00000490268.2:p.Cys158Ter
ENST00000585748.3:c.102_108del	ENSP00000477641.2:p.Cys34Ter
ENST00000585851.2:c.300_306del	ENSP00000467912.2:p.Cys100Ter
ENST00000326873.12:c.474_480del MANE Select	ENSP00000324856.6:p.Cys158Ter
ENST00000652231.1:c.474_480del	ENSP00000498804.1:p.Cys158Ter
ENST00000326873.11:c.474_480del	ENSP00000324856.6:p.Cys158Ter
ENST00000585851.1:c.300_306del	ENSP00000467912.1:p.Cys100Ter
ENST00000586243.5:c.474_480del	ENSP00000467240.2:p.Cys158Ter
ENST00000586358.5:n.297_303del
ENST00000589152.5:n.564_570del
ENST00000591133.2:n.370_376del
NM_000455.4:c.474_480del , LRG_319t1:c.474_480del	NP_000446.1:p.Cys158Ter
XM_005259617.1:c.474_480del	XP_005259674.1:p.Cys158Ter
XM_005259618.3:c.474_480del	XP_005259675.1:p.Cys158Ter
XM_011528209.1:c.252_258del	XP_011526511.1:p.Cys84Ter
XR_936204.1:n.1099_1105del
XM_005259617.3:c.474_480del	XP_005259674.1:p.Cys158Ter
XM_011528209.2:c.252_258del	XP_011526511.1:p.Cys84Ter
XR_001753738.2:n.1099_1105del
XR_001753739.1:n.1099_1105del
XR_001753740.2:n.1099_1105del
NM_000455.5:c.474_480del MANE Select	NP_000446.1:p.Cys158Ter