Canonical Allele Identifier: CA2133565789
Gene: TOGARAM1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.45073853_45073856delinsAACT , CM000676.2:g.45073853_45073856delinsAACT GRCh38
NC_000014.8:g.45543056_45543059delinsAACT , CM000676.1:g.45543056_45543059delinsAACT GRCh37
NC_000014.7:g.44612806_44612809delinsAACT NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000361462.7:c.*292_*295delinsAACT MANE Select ENSP00000354917.2:n.*292_*295delinsAACT
ENST00000361462.6:c.*292_*295delinsAACT ENSP00000354917.2:n.*292_*295delinsAACT
ENST00000361577.7:c.*292_*295delinsAACT ENSP00000355045.3:n.*292_*295delinsAACT
ENST00000557423.5:c.*2457_*2460delinsAACT ENSP00000451829.1:n.*2457_*2460delinsAACT...
NM_001308120.1:c.*292_*295delinsAACT NP_001295049.1:n.*292_*295delinsAACT
NM_015091.2:c.*292_*295delinsAACT NP_055906.2:n.*292_*295delinsAACT
NM_015091.3:c.*292_*295delinsAACT NP_055906.2:n.*292_*295delinsAACT
NR_131765.1:n.5677_5680delinsAACT
XM_011536571.1:c.*597_*600delinsAACT XP_011534873.1:n.*597_*600delinsAACT
XM_017021098.1:c.*292_*295delinsAACT XP_016876587.1:n.*292_*295delinsAACT
XM_017021099.1:c.*292_*295delinsAACT XP_016876588.1:n.*292_*295delinsAACT
XR_001750194.1:n.5941_5944delinsAACT
XR_001750195.1:n.5584_5587delinsAACT
NM_001308120.2:c.*292_*295delinsAACT MANE Select NP_001295049.1:n.*292_*295delinsAACT
NM_015091.4:c.*292_*295delinsAACT NP_055906.2:n.*292_*295delinsAACT
NR_131765.2:n.5677_5680delinsAACT