Canonical Allele Identifier: CA2582591026

Gene: STK11

Linked Data

• dbSNP Id: rs2145403815
• gnomAD v4: 19-1206711-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1206711C>T , CM000681.2:g.1206711C>T	GRCh38
NC_000019.9:g.1206710C>T , CM000681.1:g.1206710C>T	GRCh37
NC_000019.8:g.1157710C>T	NCBI36
NG_007460.2:g.22305C>T , LRG_319:g.22305C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.-203C>T	ENSP00000490268.2:n.-203C>T
ENST00000585748.3:c.-82-11706C>T	ENSP00000477641.2:n.-82-11706C>T
ENST00000326873.12:c.-203C>T MANE Select	ENSP00000324856.6:n.-203C>T
ENST00000652231.1:c.-203C>T	ENSP00000498804.1:n.-203C>T
ENST00000326873.11:c.-203C>T	ENSP00000324856.6:n.-203C>T
ENST00000585748.2:c.-82-11706C>T	ENSP00000477641.1:n.-82-11706C>T
ENST00000586243.5:c.-203C>T	ENSP00000467240.2:n.-203C>T
NM_000455.4:c.-203C>T , LRG_319t1:c.-203C>T	NP_000446.1:n.-203C>T
XM_005259617.1:c.-203C>T	XP_005259674.1:n.-203C>T
XM_005259618.3:c.-203C>T	XP_005259675.1:n.-203C>T
XM_011528209.1:c.-556C>T	XP_011526511.1:n.-556C>T
XR_936204.1:n.423C>T
XM_005259617.3:c.-203C>T	XP_005259674.1:n.-203C>T
XM_011528209.2:c.-556C>T	XP_011526511.1:n.-556C>T
XR_001753738.2:n.423C>T
XR_001753739.1:n.423C>T
XR_001753740.2:n.423C>T
NM_000455.5:c.-203C>T MANE Select	NP_000446.1:n.-203C>T