Canonical Allele Identifier: CA023359

Gene: STK11

Linked Data

• ClinVar Variation Id: 93100
• ClinVar RCV Id: RCV000078915
• dbSNP Id: rs398123406
• gnomAD v4: 19-1222984-G-T
• COSMIC: COSM5985665
• MyVariant Identifiers: chr19:g.1222983G>T (hg19) ; chr19:g.1222984G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1222984G>T , CM000681.2:g.1222984G>T	GRCh38
NC_000019.9:g.1222983G>T , CM000681.1:g.1222983G>T	GRCh37
NC_000019.8:g.1173983G>T	NCBI36
NG_007460.2:g.38578G>T , LRG_319:g.38578G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.921-1G>T	ENSP00000490268.2:n.921-1G>T
ENST00000585748.3:c.549-1G>T	ENSP00000477641.2:n.549-1G>T
ENST00000585851.2:c.747-1G>T	ENSP00000467912.2:n.747-1G>T
ENST00000326873.12:c.921-1G>T MANE Select	ENSP00000324856.6:n.921-1G>T
ENST00000652231.1:c.921-1G>T	ENSP00000498804.1:n.921-1G>T
ENST00000326873.11:c.921-1G>T	ENSP00000324856.6:n.921-1G>T
ENST00000586243.5:c.921-1G>T	ENSP00000467240.2:n.921-1G>T
ENST00000589152.5:n.1619-1G>T
ENST00000591133.2:n.892-1G>T
NM_000455.4:c.921-1G>T , LRG_319t1:c.921-1G>T	NP_000446.1:n.921-1G>T
XM_005259617.1:c.921-1G>T	XP_005259674.1:n.921-1G>T
XM_005259618.3:c.921-1G>T	XP_005259675.1:n.921-1G>T
XM_011528209.1:c.699-1G>T	XP_011526511.1:n.699-1G>T
XR_936204.1:n.1697-1G>T
XM_005259617.3:c.921-1G>T	XP_005259674.1:n.921-1G>T
XM_011528209.2:c.699-1G>T	XP_011526511.1:n.699-1G>T
XR_001753738.2:n.1727-1G>T
XR_001753739.1:n.1727-1G>T
XR_001753740.2:n.1697-1G>T
NM_000455.5:c.921-1G>T MANE Select	NP_000446.1:n.921-1G>T