Canonical Allele Identifier: CA631032283
Gene: STK11 HGNC NCBI

Linked Data

dbSNP Id: rs1282182796

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1219608_1219609insAT , CM000681.2:g.1219608_1219609insAT GRCh38
NC_000019.9:g.1219607_1219608insAT , CM000681.1:g.1219607_1219608insAT GRCh37
NC_000019.8:g.1170607_1170608insAT NCBI36
NG_007460.2:g.35202_35203insAT , LRG_319:g.35202_35203insAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000585465.3:c.464+195_464+196insAT ENSP00000490268.2:n.464+195_464+196insAT
ENST00000585748.3:c.92+195_92+196insAT ENSP00000477641.2:n.92+195_92+196insAT
ENST00000585851.2:c.291-765_291-764insAT ENSP00000467912.2:n.291-765_291-764insAT
ENST00000326873.12:c.464+195_464+196insAT MANE Select ENSP00000324856.6:n.464+195_464+196insAT
ENST00000652231.1:c.464+195_464+196insAT ENSP00000498804.1:n.464+195_464+196insAT
ENST00000326873.11:c.464+195_464+196insAT ENSP00000324856.6:n.464+195_464+196insAT
ENST00000585851.1:c.291-765_291-764insAT ENSP00000467912.1:n.291-765_291-764insAT
ENST00000586243.5:c.464+195_464+196insAT ENSP00000467240.2:n.464+195_464+196insAT
ENST00000586358.5:n.287+195_287+196insAT
ENST00000589152.5:n.554+195_554+196insAT
NM_000455.4:c.464+195_464+196insAT , LRG_319t1:c.464+195_464+196insAT NP_000446.1:n.464+195_464+196insAT
XM_005259617.1:c.464+195_464+196insAT XP_005259674.1:n.464+195_464+196insAT
XM_005259618.3:c.464+195_464+196insAT XP_005259675.1:n.464+195_464+196insAT
XM_011528209.1:c.242+195_242+196insAT XP_011526511.1:n.242+195_242+196insAT
XR_936204.1:n.1089+195_1089+196insAT
XM_005259617.3:c.464+195_464+196insAT XP_005259674.1:n.464+195_464+196insAT
XM_011528209.2:c.242+195_242+196insAT XP_011526511.1:n.242+195_242+196insAT
XR_001753738.2:n.1089+195_1089+196insAT
XR_001753739.1:n.1089+195_1089+196insAT
XR_001753740.2:n.1089+195_1089+196insAT
NM_000455.5:c.464+195_464+196insAT MANE Select NP_000446.1:n.464+195_464+196insAT