Canonical Allele Identifier: CA2624689765
Gene: TOGARAM1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.45073846C>T , CM000676.2:g.45073846C>T GRCh38
NC_000014.8:g.45543049C>T , CM000676.1:g.45543049C>T GRCh37
NC_000014.7:g.44612799C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000361462.7:c.*285C>T MANE Select ENSP00000354917.2:n.*285C>T
ENST00000361462.6:c.*285C>T ENSP00000354917.2:n.*285C>T
ENST00000361577.7:c.*285C>T ENSP00000355045.3:n.*285C>T
ENST00000557423.5:c.*2450C>T ENSP00000451829.1:n.*2450C>T
NM_001308120.1:c.*285C>T NP_001295049.1:n.*285C>T
NM_015091.2:c.*285C>T NP_055906.2:n.*285C>T
NM_015091.3:c.*285C>T NP_055906.2:n.*285C>T
NR_131765.1:n.5670C>T
XM_011536571.1:c.*590C>T XP_011534873.1:n.*590C>T
XM_017021098.1:c.*285C>T XP_016876587.1:n.*285C>T
XM_017021099.1:c.*285C>T XP_016876588.1:n.*285C>T
XR_001750194.1:n.5934C>T
XR_001750195.1:n.5577C>T
NM_001308120.2:c.*285C>T MANE Select NP_001295049.1:n.*285C>T
NM_015091.4:c.*285C>T NP_055906.2:n.*285C>T
NR_131765.2:n.5670C>T