Canonical Allele Identifier: CA023088

Gene: STK11

Linked Data

• ClinVar Variation Id: 184297
• ClinVar RCV Id: RCV000163525 ; RCV000461063 ; RCV001675646 ; RCV003907506
• dbSNP Id: rs748698151
• ExAC: 19:1206969 G / C
• gnomAD v2: 19-1206969-G-C
• gnomAD v3: 19-1206970-G-C
• gnomAD v4: 19-1206970-G-C
• MyVariant Identifiers: chr19:g.1206969G>C (hg19) ; chr19:g.1206970G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1206970G>C , CM000681.2:g.1206970G>C	GRCh38
NC_000019.9:g.1206969G>C , CM000681.1:g.1206969G>C	GRCh37
NC_000019.8:g.1157969G>C	NCBI36
NG_007460.2:g.22564G>C , LRG_319:g.22564G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000585465.3:c.57G>C	ENSP00000490268.2:p.Ser19=
ENST00000585748.3:c.-82-11447G>C	ENSP00000477641.2:n.-82-11447G>C
ENST00000585851.2:c.57G>C	ENSP00000467912.2:p.Ser19=
ENST00000326873.12:c.57G>C MANE Select	ENSP00000324856.6:p.Ser19=
ENST00000652231.1:c.57G>C	ENSP00000498804.1:p.Ser19=
ENST00000326873.11:c.57G>C	ENSP00000324856.6:p.Ser19=
ENST00000585748.2:c.-82-11447G>C	ENSP00000477641.1:n.-82-11447G>C
ENST00000585851.1:c.57G>C	ENSP00000467912.1:p.Ser19=
ENST00000586243.5:c.57G>C	ENSP00000467240.2:p.Ser19=
ENST00000589152.5:n.147G>C
ENST00000593219.5:c.57G>C	ENSP00000466610.1:p.Ser19=
NM_000455.4:c.57G>C , LRG_319t1:c.57G>C	NP_000446.1:p.Ser19=
XM_005259617.1:c.57G>C	XP_005259674.1:p.Ser19=
XM_005259618.3:c.57G>C	XP_005259675.1:p.Ser19=
XM_011528209.1:c.-297G>C	XP_011526511.1:n.-297G>C
XR_936204.1:n.682G>C
XM_005259617.3:c.57G>C	XP_005259674.1:p.Ser19=
XM_011528209.2:c.-297G>C	XP_011526511.1:n.-297G>C
XR_001753738.2:n.682G>C
XR_001753739.1:n.682G>C
XR_001753740.2:n.682G>C
NM_000455.5:c.57G>C MANE Select	NP_000446.1:p.Ser19=