Canonical Allele Identifier: CA2624689720
Gene: TOGARAM1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.45073758_45073768dup , CM000676.2:g.45073758_45073768dup GRCh38
NC_000014.8:g.45542961_45542971dup , CM000676.1:g.45542961_45542971dup GRCh37
NC_000014.7:g.44612711_44612721dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000361462.7:c.*197_*207dup MANE Select ENSP00000354917.2:n.*197_*207dup
ENST00000361462.6:c.*197_*207dup ENSP00000354917.2:n.*197_*207dup
ENST00000361577.7:c.*197_*207dup ENSP00000355045.3:n.*197_*207dup
ENST00000556823.1:c.665_675dup ENSP00000450465.1:n.665_675dup
ENST00000557423.5:c.*2362_*2372dup ENSP00000451829.1:n.*2362_*2372dup
NM_001308120.1:c.*197_*207dup NP_001295049.1:n.*197_*207dup
NM_015091.2:c.*197_*207dup NP_055906.2:n.*197_*207dup
NM_015091.3:c.*197_*207dup NP_055906.2:n.*197_*207dup
NR_131765.1:n.5582_5592dup
XM_011536571.1:c.*502_*512dup XP_011534873.1:n.*502_*512dup
XM_017021098.1:c.*197_*207dup XP_016876587.1:n.*197_*207dup
XM_017021099.1:c.*197_*207dup XP_016876588.1:n.*197_*207dup
XR_001750194.1:n.5846_5856dup
XR_001750195.1:n.5489_5499dup
NM_001308120.2:c.*197_*207dup MANE Select NP_001295049.1:n.*197_*207dup
NM_015091.4:c.*197_*207dup NP_055906.2:n.*197_*207dup
NR_131765.2:n.5582_5592dup