Canonical Allele Identifier: CA402949008

Gene: STK11

Linked Data - Expert Curation

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1220434G>C , CM000681.2:g.1220434G>C	GRCh38
NC_000019.9:g.1220433G>C , CM000681.1:g.1220433G>C	GRCh37
NC_000019.8:g.1171433G>C	NCBI36
NG_007460.2:g.36028G>C , LRG_319:g.36028G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.526G>C	ENSP00000490268.2:p.Asp176His
ENST00000585748.3:c.154G>C	ENSP00000477641.2:p.Asp52His
ENST00000585851.2:c.352G>C	ENSP00000467912.2:p.Asp118His
ENST00000326873.12:c.526G>C MANE Select	ENSP00000324856.6:p.Asp176His
ENST00000652231.1:c.526G>C	ENSP00000498804.1:p.Asp176His
ENST00000326873.11:c.526G>C	ENSP00000324856.6:p.Asp176His
ENST00000585851.1:c.352G>C	ENSP00000467912.1:p.Asp118His
ENST00000586243.5:c.526G>C	ENSP00000467240.2:p.Asp176His
ENST00000586358.5:n.349G>C
ENST00000589152.5:n.616G>C
ENST00000591133.2:n.422G>C
NM_000455.4:c.526G>C , LRG_319t1:c.526G>C	NP_000446.1:p.Asp176His
XM_005259617.1:c.526G>C	XP_005259674.1:p.Asp176His
XM_005259618.3:c.526G>C	XP_005259675.1:p.Asp176His
XM_011528209.1:c.304G>C	XP_011526511.1:p.Asp102His
XR_936204.1:n.1151G>C
XM_005259617.3:c.526G>C	XP_005259674.1:p.Asp176His
XM_011528209.2:c.304G>C	XP_011526511.1:p.Asp102His
XR_001753738.2:n.1151G>C
XR_001753739.1:n.1151G>C
XR_001753740.2:n.1151G>C
NM_000455.5:c.526G>C MANE Select	NP_000446.1:p.Asp176His