Canonical Allele Identifier: CA2582592030
Gene: STK11 HGNC NCBI

Linked Data

dbSNP Id: rs2145421922
gnomAD v4: 19-1219263-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1219263C>T , CM000681.2:g.1219263C>T GRCh38
NC_000019.9:g.1219262C>T , CM000681.1:g.1219262C>T GRCh37
NC_000019.8:g.1170262C>T NCBI36
NG_007460.2:g.34857C>T , LRG_319:g.34857C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000585465.3:c.375-61C>T ENSP00000490268.2:n.375-61C>T
ENST00000585748.3:c.3-61C>T ENSP00000477641.2:n.3-61C>T
ENST00000585851.2:c.291-1110C>T ENSP00000467912.2:n.291-1110C>T
ENST00000326873.12:c.375-61C>T MANE Select ENSP00000324856.6:n.375-61C>T
ENST00000652231.1:c.375-61C>T ENSP00000498804.1:n.375-61C>T
ENST00000326873.11:c.375-61C>T ENSP00000324856.6:n.375-61C>T
ENST00000585748.2:c.3-61C>T ENSP00000477641.1:n.3-61C>T
ENST00000585851.1:c.291-1110C>T ENSP00000467912.1:n.291-1110C>T
ENST00000586243.5:c.375-61C>T ENSP00000467240.2:n.375-61C>T
ENST00000586358.5:n.198-61C>T
ENST00000589152.5:n.465-61C>T
ENST00000593219.5:c.*200-61C>T ENSP00000466610.1:n.*200-61C>T
NM_000455.4:c.375-61C>T , LRG_319t1:c.375-61C>T NP_000446.1:n.375-61C>T
XM_005259617.1:c.375-61C>T XP_005259674.1:n.375-61C>T
XM_005259618.3:c.375-61C>T XP_005259675.1:n.375-61C>T
XM_011528209.1:c.153-61C>T XP_011526511.1:n.153-61C>T
XR_936204.1:n.1000-61C>T
XM_005259617.3:c.375-61C>T XP_005259674.1:n.375-61C>T
XM_011528209.2:c.153-61C>T XP_011526511.1:n.153-61C>T
XR_001753738.2:n.1000-61C>T
XR_001753739.1:n.1000-61C>T
XR_001753740.2:n.1000-61C>T
NM_000455.5:c.375-61C>T MANE Select NP_000446.1:n.375-61C>T