Canonical Allele Identifier: CA2582597188

Gene: STK11

Linked Data

• dbSNP Id: rs2145436743
• gnomAD v4: 19-1226663-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1226663G>A , CM000681.2:g.1226663G>A	GRCh38
NC_000019.9:g.1226662G>A , CM000681.1:g.1226662G>A	GRCh37
NC_000019.8:g.1177662G>A	NCBI36
NG_007460.2:g.42257G>A , LRG_319:g.42257G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.*2919G>A	ENSP00000490268.2:n.*2919G>A
ENST00000585748.3:c.*16G>A	ENSP00000477641.2:n.*16G>A
ENST00000585851.2:c.*16G>A	ENSP00000467912.2:n.*16G>A
ENST00000326873.12:c.*16G>A MANE Select	ENSP00000324856.6:n.*16G>A
ENST00000326873.11:c.*16G>A	ENSP00000324856.6:n.*16G>A
ENST00000585465.2:n.3051G>A
ENST00000586243.5:c.*16G>A	ENSP00000467240.2:n.*16G>A
ENST00000589152.5:n.2016G>A
NM_000455.4:c.*16G>A , LRG_319t1:c.*16G>A	NP_000446.1:n.*16G>A
XM_005259617.1:c.1313G>A	XP_005259674.1:p.Ser438Asn
XM_011528209.1:c.1091G>A	XP_011526511.1:p.Ser364Asn
XM_005259617.3:c.1313G>A	XP_005259674.1:p.Ser438Asn
XM_011528209.2:c.1091G>A	XP_011526511.1:p.Ser364Asn
XR_001753738.2:n.2124G>A
XR_001753740.2:n.2094G>A
NM_000455.5:c.*16G>A MANE Select	NP_000446.1:n.*16G>A