Canonical Allele Identifier: CA504707683

Gene: STK11

Linked Data

• ClinVar Variation Id: 926174
• ClinVar RCV Id: RCV001188573
• dbSNP Id: rs587781178
• gnomAD v4: 19-1221968-G-C
• MyVariant Identifiers: chr19:g.1221967G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1221968G>C , CM000681.2:g.1221968G>C	GRCh38
NC_000019.9:g.1221967G>C , CM000681.1:g.1221967G>C	GRCh37
NC_000019.8:g.1172967G>C	NCBI36
NG_007460.2:g.37562G>C , LRG_319:g.37562G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.882G>C	ENSP00000490268.2:p.Pro294=
ENST00000585748.3:c.510G>C	ENSP00000477641.2:p.Pro170=
ENST00000585851.2:c.708G>C	ENSP00000467912.2:p.Pro236=
ENST00000326873.12:c.882G>C MANE Select	ENSP00000324856.6:p.Pro294=
ENST00000652231.1:c.882G>C	ENSP00000498804.1:p.Pro294=
ENST00000326873.11:c.882G>C	ENSP00000324856.6:p.Pro294=
ENST00000586243.5:c.882G>C	ENSP00000467240.2:p.Pro294=
ENST00000589152.5:n.1580G>C
ENST00000591133.2:n.853G>C
NM_000455.4:c.882G>C , LRG_319t1:c.882G>C	NP_000446.1:p.Pro294=
XM_005259617.1:c.882G>C	XP_005259674.1:p.Pro294=
XM_005259618.3:c.882G>C	XP_005259675.1:p.Pro294=
XM_011528209.1:c.660G>C	XP_011526511.1:p.Pro220=
XR_936204.1:n.1658G>C
XM_005259617.3:c.882G>C	XP_005259674.1:p.Pro294=
XM_011528209.2:c.660G>C	XP_011526511.1:p.Pro220=
XR_001753738.2:n.1688G>C
XR_001753739.1:n.1688G>C
XR_001753740.2:n.1658G>C
NM_000455.5:c.882G>C MANE Select	NP_000446.1:p.Pro294=