Canonical Allele Identifier: CA16608848

Gene: STK11

Linked Data

• ClinVar Variation Id: 383537
• ClinVar RCV Id: RCV000428614 ; RCV001017439 ; RCV001436137
• dbSNP Id: rs1057521658
• MyVariant Identifiers: chr19:g.1226484T>C (hg19) ; chr19:g.1226485T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1226485T>C , CM000681.2:g.1226485T>C	GRCh38
NC_000019.9:g.1226484T>C , CM000681.1:g.1226484T>C	GRCh37
NC_000019.8:g.1177484T>C	NCBI36
NG_007460.2:g.42079T>C , LRG_319:g.42079T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.*2741T>C	ENSP00000490268.2:n.*2741T>C
ENST00000585748.3:c.768T>C	ENSP00000477641.2:p.Asn256=
ENST00000585851.2:c.966T>C	ENSP00000467912.2:p.Asn322=
ENST00000326873.12:c.1140T>C MANE Select	ENSP00000324856.6:p.Asn380=
ENST00000326873.11:c.1140T>C	ENSP00000324856.6:p.Asn380=
ENST00000585465.2:n.2873T>C
ENST00000586243.5:c.1140T>C	ENSP00000467240.2:p.Asn380=
ENST00000589152.5:n.1838T>C
NM_000455.4:c.1140T>C , LRG_319t1:c.1140T>C	NP_000446.1:p.Asn380=
XM_005259617.1:c.1135T>C	XP_005259674.1:p.Trp379Arg
XM_011528209.1:c.913T>C	XP_011526511.1:p.Trp305Arg
XM_005259617.3:c.1135T>C	XP_005259674.1:p.Trp379Arg
XM_011528209.2:c.913T>C	XP_011526511.1:p.Trp305Arg
XR_001753738.2:n.1946T>C
XR_001753740.2:n.1916T>C
NM_000455.5:c.1140T>C MANE Select	NP_000446.1:p.Asn380=