Canonical Allele Identifier: CA504707278

Gene: STK11

Linked Data

• ClinVar Variation Id: 759552
• ClinVar RCV Id: RCV001183184 ; RCV001503767
• dbSNP Id: rs1599927695
• MyVariant Identifiers: chr19:g.1221311T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1221312T>C , CM000681.2:g.1221312T>C	GRCh38
NC_000019.9:g.1221311T>C , CM000681.1:g.1221311T>C	GRCh37
NC_000019.8:g.1172311T>C	NCBI36
NG_007460.2:g.36906T>C , LRG_319:g.36906T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.834T>C	ENSP00000490268.2:p.Cys278=
ENST00000585748.3:c.462T>C	ENSP00000477641.2:p.Cys154=
ENST00000585851.2:c.660T>C	ENSP00000467912.2:p.Cys220=
ENST00000326873.12:c.834T>C MANE Select	ENSP00000324856.6:p.Cys278=
ENST00000652231.1:c.834T>C	ENSP00000498804.1:p.Cys278=
ENST00000326873.11:c.834T>C	ENSP00000324856.6:p.Cys278=
ENST00000586243.5:c.834T>C	ENSP00000467240.2:p.Cys278=
ENST00000586358.5:n.732T>C
ENST00000589152.5:n.924T>C
ENST00000591133.2:n.805T>C
NM_000455.4:c.834T>C , LRG_319t1:c.834T>C	NP_000446.1:p.Cys278=
XM_005259617.1:c.834T>C	XP_005259674.1:p.Cys278=
XM_005259618.3:c.834T>C	XP_005259675.1:p.Cys278=
XM_011528209.1:c.612T>C	XP_011526511.1:p.Cys204=
XR_936204.1:n.1459T>C
XM_005259617.3:c.834T>C	XP_005259674.1:p.Cys278=
XM_011528209.2:c.612T>C	XP_011526511.1:p.Cys204=
XR_001753738.2:n.1459T>C
XR_001753739.1:n.1459T>C
XR_001753740.2:n.1459T>C
NM_000455.5:c.834T>C MANE Select	NP_000446.1:p.Cys278=