Canonical Allele Identifier: CA2624689733
Gene: TOGARAM1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.45073779A>G , CM000676.2:g.45073779A>G GRCh38
NC_000014.8:g.45542982A>G , CM000676.1:g.45542982A>G GRCh37
NC_000014.7:g.44612732A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000361462.7:c.*218A>G MANE Select ENSP00000354917.2:n.*218A>G
ENST00000361462.6:c.*218A>G ENSP00000354917.2:n.*218A>G
ENST00000361577.7:c.*218A>G ENSP00000355045.3:n.*218A>G
ENST00000556823.1:c.686A>G ENSP00000450465.1:n.686A>G
ENST00000557423.5:c.*2383A>G ENSP00000451829.1:n.*2383A>G
NM_001308120.1:c.*218A>G NP_001295049.1:n.*218A>G
NM_015091.2:c.*218A>G NP_055906.2:n.*218A>G
NM_015091.3:c.*218A>G NP_055906.2:n.*218A>G
NR_131765.1:n.5603A>G
XM_011536571.1:c.*523A>G XP_011534873.1:n.*523A>G
XM_017021098.1:c.*218A>G XP_016876587.1:n.*218A>G
XM_017021099.1:c.*218A>G XP_016876588.1:n.*218A>G
XR_001750194.1:n.5867A>G
XR_001750195.1:n.5510A>G
NM_001308120.2:c.*218A>G MANE Select NP_001295049.1:n.*218A>G
NM_015091.4:c.*218A>G NP_055906.2:n.*218A>G
NR_131765.2:n.5603A>G