Canonical Allele Identifier: CA023318

Gene: STK11

Linked Data

• ClinVar Variation Id: 182886
• ClinVar RCV Id: RCV000160978 ; RCV000196327 ; RCV000213022 ; RCV002510800
• dbSNP Id: rs148928808
• ExAC: 19:1221961 C / T
• gnomAD v2: 19-1221961-C-T
• gnomAD v3: 19-1221962-C-T
• gnomAD v4: 19-1221962-C-T
• MyVariant Identifiers: chr19:g.1221961C>T (hg19) ; chr19:g.1221962C>T (hg38)
• PubMed: PMID:12372054

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1221962C>T , CM000681.2:g.1221962C>T	GRCh38
NC_000019.9:g.1221961C>T , CM000681.1:g.1221961C>T	GRCh37
NC_000019.8:g.1172961C>T	NCBI36
NG_007460.2:g.37556C>T , LRG_319:g.37556C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000585465.3:c.876C>T	ENSP00000490268.2:p.Tyr292=
ENST00000585748.3:c.504C>T	ENSP00000477641.2:p.Tyr168=
ENST00000585851.2:c.702C>T	ENSP00000467912.2:p.Tyr234=
ENST00000326873.12:c.876C>T MANE Select	ENSP00000324856.6:p.Tyr292=
ENST00000652231.1:c.876C>T	ENSP00000498804.1:p.Tyr292=
ENST00000326873.11:c.876C>T	ENSP00000324856.6:p.Tyr292=
ENST00000586243.5:c.876C>T	ENSP00000467240.2:p.Tyr292=
ENST00000589152.5:n.1574C>T
ENST00000591133.2:n.847C>T
NM_000455.4:c.876C>T , LRG_319t1:c.876C>T	NP_000446.1:p.Tyr292=
XM_005259617.1:c.876C>T	XP_005259674.1:p.Tyr292=
XM_005259618.3:c.876C>T	XP_005259675.1:p.Tyr292=
XM_011528209.1:c.654C>T	XP_011526511.1:p.Tyr218=
XR_936204.1:n.1652C>T
XM_005259617.3:c.876C>T	XP_005259674.1:p.Tyr292=
XM_011528209.2:c.654C>T	XP_011526511.1:p.Tyr218=
XR_001753738.2:n.1682C>T
XR_001753739.1:n.1682C>T
XR_001753740.2:n.1652C>T
NM_000455.5:c.876C>T MANE Select	NP_000446.1:p.Tyr292=