Canonical Allele Identifier: CA919408032
Gene: TOGARAM1 HGNC NCBI

Linked Data

dbSNP Id: rs1594715391

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.45073900del , CM000676.2:g.45073900del GRCh38
NC_000014.8:g.45543103del , CM000676.1:g.45543103del GRCh37
NC_000014.7:g.44612853del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000361462.7:c.*339del MANE Select ENSP00000354917.2:n.*339del
ENST00000361462.6:c.*339del ENSP00000354917.2:n.*339del
ENST00000361577.7:c.*339del ENSP00000355045.3:n.*339del
ENST00000557423.5:c.*2504del ENSP00000451829.1:n.*2504del
NM_001308120.1:c.*339del NP_001295049.1:n.*339del
NM_015091.2:c.*339del NP_055906.2:n.*339del
NM_015091.3:c.*339del NP_055906.2:n.*339del
NR_131765.1:n.5724del
XM_011536571.1:c.*644del XP_011534873.1:n.*644del
XM_017021098.1:c.*339del XP_016876587.1:n.*339del
XM_017021099.1:c.*339del XP_016876588.1:n.*339del
XR_001750194.1:n.5988del
XR_001750195.1:n.5631del
NM_001308120.2:c.*339del MANE Select NP_001295049.1:n.*339del
NM_015091.4:c.*339del NP_055906.2:n.*339del
NR_131765.2:n.5724del