Canonical Allele Identifier: CA402953906

Gene: STK11

Linked Data

• dbSNP Id: rs786201309
• gnomAD v4: 19-1226580-A-C
• MyVariant Identifiers: chr19:g.1226579A>C (hg19) ; chr19:g.1226580A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1226580A>C , CM000681.2:g.1226580A>C	GRCh38
NC_000019.9:g.1226579A>C , CM000681.1:g.1226579A>C	GRCh37
NC_000019.8:g.1177579A>C	NCBI36
NG_007460.2:g.42174A>C , LRG_319:g.42174A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.*2836A>C	ENSP00000490268.2:n.*2836A>C
ENST00000585748.3:c.863A>C	ENSP00000477641.2:p.Asn288Thr
ENST00000585851.2:c.1061A>C	ENSP00000467912.2:p.Asn354Thr
ENST00000326873.12:c.1235A>C MANE Select	ENSP00000324856.6:p.Asn412Thr
ENST00000326873.11:c.1235A>C	ENSP00000324856.6:p.Asn412Thr
ENST00000585465.2:n.2968A>C
ENST00000586243.5:c.1234A>C	ENSP00000467240.2:p.Thr412Pro
ENST00000589152.5:n.1933A>C
NM_000455.4:c.1235A>C , LRG_319t1:c.1235A>C	NP_000446.1:p.Asn412Thr
XM_005259617.1:c.1230A>C	XP_005259674.1:p.Gln410His
XM_011528209.1:c.1008A>C	XP_011526511.1:p.Gln336His
XM_005259617.3:c.1230A>C	XP_005259674.1:p.Gln410His
XM_011528209.2:c.1008A>C	XP_011526511.1:p.Gln336His
XR_001753738.2:n.2041A>C
XR_001753740.2:n.2011A>C
NM_000455.5:c.1235A>C MANE Select	NP_000446.1:p.Asn412Thr