Canonical Allele Identifier: CA402949571
Gene: STK11 HGNC NCBI

Linked Data

ClinVar Variation Id: 428759
ClinVar RCV Id: RCV000492400 RCV001269112
dbSNP Id: rs1131690923
MyVariant Identifiers: chr19:g.1220622C>T (hg19) chr19:g.1220623C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1220623C>T , CM000681.2:g.1220623C>T GRCh38
NC_000019.9:g.1220622C>T , CM000681.1:g.1220622C>T GRCh37
NC_000019.8:g.1171622C>T NCBI36
NG_007460.2:g.36217C>T , LRG_319:g.36217C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000585465.3:c.640C>T ENSP00000490268.2:p.Gln214Ter
ENST00000585748.3:c.268C>T ENSP00000477641.2:p.Gln90Ter
ENST00000585851.2:c.466C>T ENSP00000467912.2:p.Gln156Ter
ENST00000326873.12:c.640C>T MANE Select ENSP00000324856.6:p.Gln214Ter
ENST00000652231.1:c.640C>T ENSP00000498804.1:p.Gln214Ter
ENST00000326873.11:c.640C>T ENSP00000324856.6:p.Gln214Ter
ENST00000586243.5:c.640C>T ENSP00000467240.2:p.Gln214Ter
ENST00000586358.5:n.538C>T
ENST00000589152.5:n.730C>T
ENST00000591133.2:n.611C>T
NM_000455.4:c.640C>T , LRG_319t1:c.640C>T NP_000446.1:p.Gln214Ter
XM_005259617.1:c.640C>T XP_005259674.1:p.Gln214Ter
XM_005259618.3:c.640C>T XP_005259675.1:p.Gln214Ter
XM_011528209.1:c.418C>T XP_011526511.1:p.Gln140Ter
XR_936204.1:n.1265C>T
XM_005259617.3:c.640C>T XP_005259674.1:p.Gln214Ter
XM_011528209.2:c.418C>T XP_011526511.1:p.Gln140Ter
XR_001753738.2:n.1265C>T
XR_001753739.1:n.1265C>T
XR_001753740.2:n.1265C>T
NM_000455.5:c.640C>T MANE Select NP_000446.1:p.Gln214Ter
Search 100 bp 5'
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