Canonical Allele Identifier: CA048273

Gene: STK11

Linked Data

• dbSNP Id: rs758946452
• ExAC: 19:1220558 G / A
• gnomAD v2: 19-1220558-G-A
• gnomAD v4: 19-1220559-G-A
• MyVariant Identifiers: chr19:g.1220558G>A (hg19) ; chr19:g.1220559G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1220559G>A , CM000681.2:g.1220559G>A	GRCh38
NC_000019.9:g.1220558G>A , CM000681.1:g.1220558G>A	GRCh37
NC_000019.8:g.1171558G>A	NCBI36
NG_007460.2:g.36153G>A , LRG_319:g.36153G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000585465.3:c.598-22G>A	ENSP00000490268.2:n.598-22G>A
ENST00000585748.3:c.226-22G>A	ENSP00000477641.2:n.226-22G>A
ENST00000585851.2:c.424-22G>A	ENSP00000467912.2:n.424-22G>A
ENST00000326873.12:c.598-22G>A MANE Select	ENSP00000324856.6:n.598-22G>A
ENST00000652231.1:c.598-22G>A	ENSP00000498804.1:n.598-22G>A
ENST00000326873.11:c.598-22G>A	ENSP00000324856.6:n.598-22G>A
ENST00000585851.1:c.424-22G>A	ENSP00000467912.1:n.424-22G>A
ENST00000586243.5:c.598-22G>A	ENSP00000467240.2:n.598-22G>A
ENST00000586358.5:n.474G>A
ENST00000589152.5:n.688-22G>A
ENST00000591133.2:n.547G>A
NM_000455.4:c.598-22G>A , LRG_319t1:c.598-22G>A	NP_000446.1:n.598-22G>A
XM_005259617.1:c.598-22G>A	XP_005259674.1:n.598-22G>A
XM_005259618.3:c.598-22G>A	XP_005259675.1:n.598-22G>A
XM_011528209.1:c.376-22G>A	XP_011526511.1:n.376-22G>A
XR_936204.1:n.1223-22G>A
XM_005259617.3:c.598-22G>A	XP_005259674.1:n.598-22G>A
XM_011528209.2:c.376-22G>A	XP_011526511.1:n.376-22G>A
XR_001753738.2:n.1223-22G>A
XR_001753739.1:n.1223-22G>A
XR_001753740.2:n.1223-22G>A
NM_000455.5:c.598-22G>A MANE Select	NP_000446.1:n.598-22G>A