Canonical Allele Identifier: CA783311986

Gene: STK11

Linked Data

• dbSNP Id: rs965575193
• gnomAD v3: 19-1206772-C-G
• gnomAD v4: 19-1206772-C-G
• MyVariant Identifiers: chr19:g.1206771C>G (hg19) ; chr19:g.1206772C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1206772C>G , CM000681.2:g.1206772C>G	GRCh38
NC_000019.9:g.1206771C>G , CM000681.1:g.1206771C>G	GRCh37
NC_000019.8:g.1157771C>G	NCBI36
NG_007460.2:g.22366C>G , LRG_319:g.22366C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000585465.3:c.-142C>G	ENSP00000490268.2:n.-142C>G
ENST00000585748.3:c.-82-11645C>G	ENSP00000477641.2:n.-82-11645C>G
ENST00000326873.12:c.-142C>G MANE Select	ENSP00000324856.6:n.-142C>G
ENST00000652231.1:c.-142C>G	ENSP00000498804.1:n.-142C>G
ENST00000326873.11:c.-142C>G	ENSP00000324856.6:n.-142C>G
ENST00000585748.2:c.-82-11645C>G	ENSP00000477641.1:n.-82-11645C>G
ENST00000586243.5:c.-142C>G	ENSP00000467240.2:n.-142C>G
NM_000455.4:c.-142C>G , LRG_319t1:c.-142C>G	NP_000446.1:n.-142C>G
XM_005259617.1:c.-142C>G	XP_005259674.1:n.-142C>G
XM_005259618.3:c.-142C>G	XP_005259675.1:n.-142C>G
XM_011528209.1:c.-495C>G	XP_011526511.1:n.-495C>G
XR_936204.1:n.484C>G
XM_005259617.3:c.-142C>G	XP_005259674.1:n.-142C>G
XM_011528209.2:c.-495C>G	XP_011526511.1:n.-495C>G
XR_001753738.2:n.484C>G
XR_001753739.1:n.484C>G
XR_001753740.2:n.484C>G
NM_000455.5:c.-142C>G MANE Select	NP_000446.1:n.-142C>G