Canonical Allele Identifier: CA402953540

Gene: STK11

Linked Data

• ClinVar Variation Id: 2850565
• ClinVar RCV Id: RCV003617445
• dbSNP Id: rs2145436083
• MyVariant Identifiers: chr19:g.1226521A>T (hg19) ; chr19:g.1226522A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1226522A>T , CM000681.2:g.1226522A>T	GRCh38
NC_000019.9:g.1226521A>T , CM000681.1:g.1226521A>T	GRCh37
NC_000019.8:g.1177521A>T	NCBI36
NG_007460.2:g.42116A>T , LRG_319:g.42116A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.*2778A>T	ENSP00000490268.2:n.*2778A>T
ENST00000585748.3:c.805A>T	ENSP00000477641.2:p.Asn269Tyr
ENST00000585851.2:c.1003A>T	ENSP00000467912.2:p.Asn335Tyr
ENST00000326873.12:c.1177A>T MANE Select	ENSP00000324856.6:p.Asn393Tyr
ENST00000326873.11:c.1177A>T	ENSP00000324856.6:p.Asn393Tyr
ENST00000585465.2:n.2910A>T
ENST00000586243.5:c.1177A>T	ENSP00000467240.2:p.Asn393Tyr
ENST00000589152.5:n.1875A>T
NM_000455.4:c.1177A>T , LRG_319t1:c.1177A>T	NP_000446.1:p.Asn393Tyr
XM_005259617.1:c.1172A>T	XP_005259674.1:p.Glu391Val
XM_011528209.1:c.950A>T	XP_011526511.1:p.Glu317Val
XM_005259617.3:c.1172A>T	XP_005259674.1:p.Glu391Val
XM_011528209.2:c.950A>T	XP_011526511.1:p.Glu317Val
XR_001753738.2:n.1983A>T
XR_001753740.2:n.1953A>T
NM_000455.5:c.1177A>T MANE Select	NP_000446.1:p.Asn393Tyr