Canonical Allele Identifier: CA658684207
Community Standard Title: NM_000455.5(STK11):c.597+18_597+19delinsTGCTA
Gene: STK11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1220523_1220524delinsTGCTA , CM000681.2:g.1220523_1220524delinsTGCTA GRCh38
NC_000019.9:g.1220522_1220523delinsTGCTA , CM000681.1:g.1220522_1220523delinsTGCTA GRCh37
NC_000019.8:g.1171522_1171523delinsTGCTA NCBI36
NG_007460.2:g.36117_36118delinsTGCTA , LRG_319:g.36117_36118delinsTGCTA

Transcript Alleles

HGVS Amino-acid Change
NM_000455.5:c.597+18_597+19delinsTGCTA MANE Select NP_000446.1:n.597+18_597+19delinsTGCTA
ENST00000326873.12:c.597+18_597+19delinsTGCTA MANE Select ENSP00000324856.6:n.597+18_597+19delinsTGCTA
NM_000455.4:c.597+18_597+19delinsTGCTA , LRG_319t1:c.597+18_597+19delinsTGCTA NP_000446.1:n.597+18_597+19delinsTGCTA
ENST00000326873.11:c.597+18_597+19delinsTGCTA ENSP00000324856.6:n.597+18_597+19delinsTGCTA
ENST00000585465.3:c.597+18_597+19delinsTGCTA ENSP00000490268.2:n.597+18_597+19delinsTGCTA
ENST00000585748.3:c.225+18_225+19delinsTGCTA ENSP00000477641.2:n.225+18_225+19delinsTGCTA
ENST00000585851.1:c.423+18_423+19delinsTGCTA ENSP00000467912.1:n.423+18_423+19delinsTGCTA
ENST00000585851.2:c.423+18_423+19delinsTGCTA ENSP00000467912.2:n.423+18_423+19delinsTGCTA
ENST00000586243.5:c.597+18_597+19delinsTGCTA ENSP00000467240.2:n.597+18_597+19delinsTGCTA
ENST00000586358.5:n.438_439delinsTGCTA
ENST00000589152.5:n.687+18_687+19delinsTGCTA
ENST00000591133.2:n.511_512delinsTGCTA
ENST00000652231.1:c.597+18_597+19delinsTGCTA ENSP00000498804.1:n.597+18_597+19delinsTGCTA
XM_005259617.1:c.597+18_597+19delinsTGCTA XP_005259674.1:n.597+18_597+19delinsTGCTA
XM_005259617.3:c.597+18_597+19delinsTGCTA XP_005259674.1:n.597+18_597+19delinsTGCTA
XM_005259618.3:c.597+18_597+19delinsTGCTA XP_005259675.1:n.597+18_597+19delinsTGCTA
XM_011528209.1:c.375+18_375+19delinsTGCTA XP_011526511.1:n.375+18_375+19delinsTGCTA
XM_011528209.2:c.375+18_375+19delinsTGCTA XP_011526511.1:n.375+18_375+19delinsTGCTA
XR_001753738.2:n.1222+18_1222+19delinsTGCTA
XR_001753739.1:n.1222+18_1222+19delinsTGCTA
XR_001753740.2:n.1222+18_1222+19delinsTGCTA
XR_936204.1:n.1222+18_1222+19delinsTGCTA