Canonical Allele Identifier: CA2133565779
Gene: TOGARAM1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.45073849T= , CM000676.2:g.45073849T= GRCh38
NC_000014.8:g.45543052T= , CM000676.1:g.45543052T= GRCh37
NC_000014.7:g.44612802T= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000361462.7:c.*288T= MANE Select ENSP00000354917.2:n.*288T=
ENST00000361462.6:c.*288T= ENSP00000354917.2:n.*288T=
ENST00000361577.7:c.*288T= ENSP00000355045.3:n.*288T=
ENST00000557423.5:c.*2453T= ENSP00000451829.1:n.*2453T=
NM_001308120.1:c.*288T= NP_001295049.1:n.*288T=
NM_015091.2:c.*288T= NP_055906.2:n.*288T=
NM_015091.3:c.*288T= NP_055906.2:n.*288T=
NR_131765.1:n.5673T=
XM_011536571.1:c.*593T= XP_011534873.1:n.*593T=
XM_017021098.1:c.*288T= XP_016876587.1:n.*288T=
XM_017021099.1:c.*288T= XP_016876588.1:n.*288T=
XR_001750194.1:n.5937T=
XR_001750195.1:n.5580T=
NM_001308120.2:c.*288T= MANE Select NP_001295049.1:n.*288T=
NM_015091.4:c.*288T= NP_055906.2:n.*288T=
NR_131765.2:n.5673T=