Canonical Allele Identifier: CA2695227886

Gene: STK11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1220377_1220406del , CM000681.2:g.1220377_1220406del	GRCh38
NC_000019.9:g.1220376_1220405del , CM000681.1:g.1220376_1220405del	GRCh37
NC_000019.8:g.1171376_1171405del	NCBI36
NG_007460.2:g.35971_36000del , LRG_319:g.35971_36000del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.469_498del	ENSP00000490268.2:p.Phe157_Tyr166del
ENST00000585748.3:c.97_126del	ENSP00000477641.2:p.Phe33_Tyr42del
ENST00000585851.2:c.295_324del	ENSP00000467912.2:p.Phe99_Tyr108del
ENST00000326873.12:c.469_498del MANE Select	ENSP00000324856.6:p.Phe157_Tyr166del
ENST00000652231.1:c.469_498del	ENSP00000498804.1:p.Phe157_Tyr166del
ENST00000326873.11:c.469_498del	ENSP00000324856.6:p.Phe157_Tyr166del
ENST00000585851.1:c.295_324del	ENSP00000467912.1:p.Phe99_Tyr108del
ENST00000586243.5:c.469_498del	ENSP00000467240.2:p.Phe157_Tyr166del
ENST00000586358.5:n.292_321del
ENST00000589152.5:n.559_588del
ENST00000591133.2:n.365_394del
NM_000455.4:c.469_498del , LRG_319t1:c.469_498del	NP_000446.1:p.Phe157_Tyr166del
XM_005259617.1:c.469_498del	XP_005259674.1:p.Phe157_Tyr166del
XM_005259618.3:c.469_498del	XP_005259675.1:p.Phe157_Tyr166del
XM_011528209.1:c.247_276del	XP_011526511.1:p.Phe83_Tyr92del
XR_936204.1:n.1094_1123del
XM_005259617.3:c.469_498del	XP_005259674.1:p.Phe157_Tyr166del
XM_011528209.2:c.247_276del	XP_011526511.1:p.Phe83_Tyr92del
XR_001753738.2:n.1094_1123del
XR_001753739.1:n.1094_1123del
XR_001753740.2:n.1094_1123del
NM_000455.5:c.469_498del MANE Select	NP_000446.1:p.Phe157_Tyr166del