Canonical Allele Identifier: CA2624689774
Gene: TOGARAM1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.45073866T>G , CM000676.2:g.45073866T>G GRCh38
NC_000014.8:g.45543069T>G , CM000676.1:g.45543069T>G GRCh37
NC_000014.7:g.44612819T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000361462.7:c.*305T>G MANE Select ENSP00000354917.2:n.*305T>G
ENST00000361462.6:c.*305T>G ENSP00000354917.2:n.*305T>G
ENST00000361577.7:c.*305T>G ENSP00000355045.3:n.*305T>G
ENST00000557423.5:c.*2470T>G ENSP00000451829.1:n.*2470T>G
NM_001308120.1:c.*305T>G NP_001295049.1:n.*305T>G
NM_015091.2:c.*305T>G NP_055906.2:n.*305T>G
NM_015091.3:c.*305T>G NP_055906.2:n.*305T>G
NR_131765.1:n.5690T>G
XM_011536571.1:c.*610T>G XP_011534873.1:n.*610T>G
XM_017021098.1:c.*305T>G XP_016876587.1:n.*305T>G
XM_017021099.1:c.*305T>G XP_016876588.1:n.*305T>G
XR_001750194.1:n.5954T>G
XR_001750195.1:n.5597T>G
NM_001308120.2:c.*305T>G MANE Select NP_001295049.1:n.*305T>G
NM_015091.4:c.*305T>G NP_055906.2:n.*305T>G
NR_131765.2:n.5690T>G