Canonical Allele Identifier: CA2528982982
Gene: TOGARAM1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.45073849_45073850dup , CM000676.2:g.45073849_45073850dup GRCh38
NC_000014.8:g.45543052_45543053dup , CM000676.1:g.45543052_45543053dup GRCh37
NC_000014.7:g.44612802_44612803dup NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000361462.7:c.*288_*289dup MANE Select ENSP00000354917.2:n.*288_*289dup
ENST00000361462.6:c.*288_*289dup ENSP00000354917.2:n.*288_*289dup
ENST00000361577.7:c.*288_*289dup ENSP00000355045.3:n.*288_*289dup
ENST00000557423.5:c.*2453_*2454dup ENSP00000451829.1:n.*2453_*2454dup
NM_001308120.1:c.*288_*289dup NP_001295049.1:n.*288_*289dup
NM_015091.2:c.*288_*289dup NP_055906.2:n.*288_*289dup
NM_015091.3:c.*288_*289dup NP_055906.2:n.*288_*289dup
NR_131765.1:n.5673_5674dup
XM_011536571.1:c.*593_*594dup XP_011534873.1:n.*593_*594dup
XM_017021098.1:c.*288_*289dup XP_016876587.1:n.*288_*289dup
XM_017021099.1:c.*288_*289dup XP_016876588.1:n.*288_*289dup
XR_001750194.1:n.5937_5938dup
XR_001750195.1:n.5580_5581dup
NM_001308120.2:c.*288_*289dup MANE Select NP_001295049.1:n.*288_*289dup
NM_015091.4:c.*288_*289dup NP_055906.2:n.*288_*289dup
NR_131765.2:n.5673_5674dup