Canonical Allele Identifier: CA783311908

Gene: STK11

Linked Data

• dbSNP Id: rs1487366773
• gnomAD v4: 19-1206651-C-G
• MyVariant Identifiers: chr19:g.1206650C>G (hg19) ; chr19:g.1206651C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1206651C>G , CM000681.2:g.1206651C>G	GRCh38
NC_000019.9:g.1206650C>G , CM000681.1:g.1206650C>G	GRCh37
NC_000019.8:g.1157650C>G	NCBI36
NG_007460.2:g.22245C>G , LRG_319:g.22245C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000585465.3:c.-263C>G	ENSP00000490268.2:n.-263C>G
ENST00000585748.3:c.-82-11766C>G	ENSP00000477641.2:n.-82-11766C>G
ENST00000326873.12:c.-263C>G MANE Select	ENSP00000324856.6:n.-263C>G
ENST00000652231.1:c.-263C>G	ENSP00000498804.1:n.-263C>G
ENST00000326873.11:c.-263C>G	ENSP00000324856.6:n.-263C>G
ENST00000585748.2:c.-82-11766C>G	ENSP00000477641.1:n.-82-11766C>G
ENST00000586243.5:c.-263C>G	ENSP00000467240.2:n.-263C>G
NM_000455.4:c.-263C>G , LRG_319t1:c.-263C>G	NP_000446.1:n.-263C>G
XM_005259617.1:c.-263C>G	XP_005259674.1:n.-263C>G
XM_005259618.3:c.-263C>G	XP_005259675.1:n.-263C>G
XM_011528209.1:c.-616C>G	XP_011526511.1:n.-616C>G
XR_936204.1:n.363C>G
XM_005259617.3:c.-263C>G	XP_005259674.1:n.-263C>G
XM_011528209.2:c.-616C>G	XP_011526511.1:n.-616C>G
XR_001753738.2:n.363C>G
XR_001753739.1:n.363C>G
XR_001753740.2:n.363C>G
NM_000455.5:c.-263C>G MANE Select	NP_000446.1:n.-263C>G