Canonical Allele Identifier: CA402953373

Gene: STK11

Linked Data

• ClinVar Variation Id: 1913842
• ClinVar RCV Id: RCV002590002
• dbSNP Id: rs730881990
• MyVariant Identifiers: chr19:g.1226492G>C (hg19) ; chr19:g.1226493G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1226493G>C , CM000681.2:g.1226493G>C	GRCh38
NC_000019.9:g.1226492G>C , CM000681.1:g.1226492G>C	GRCh37
NC_000019.8:g.1177492G>C	NCBI36
NG_007460.2:g.42087G>C , LRG_319:g.42087G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.*2749G>C	ENSP00000490268.2:n.*2749G>C
ENST00000585748.3:c.776G>C	ENSP00000477641.2:p.Arg259Pro
ENST00000585851.2:c.974G>C	ENSP00000467912.2:p.Arg325Pro
ENST00000326873.12:c.1148G>C MANE Select	ENSP00000324856.6:p.Arg383Pro
ENST00000326873.11:c.1148G>C	ENSP00000324856.6:p.Arg383Pro
ENST00000585465.2:n.2881G>C
ENST00000586243.5:c.1148G>C	ENSP00000467240.2:p.Arg383Pro
ENST00000589152.5:n.1846G>C
NM_000455.4:c.1148G>C , LRG_319t1:c.1148G>C	NP_000446.1:p.Arg383Pro
XM_005259617.1:c.1143G>C	XP_005259674.1:p.Ala381=
XM_011528209.1:c.921G>C	XP_011526511.1:p.Ala307=
XM_005259617.3:c.1143G>C	XP_005259674.1:p.Ala381=
XM_011528209.2:c.921G>C	XP_011526511.1:p.Ala307=
XR_001753738.2:n.1954G>C
XR_001753740.2:n.1924G>C
NM_000455.5:c.1148G>C MANE Select	NP_000446.1:p.Arg383Pro