Canonical Allele Identifier: CA2612995269
Gene: CCDC73 HGNC NCBI
EIF3M HGNC NCBI

Linked Data

gnomAD v4: 11-32604364-GTCTCCCAAAGTTC-G
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.32604366_32604378del , CM000673.2:g.32604366_32604378del GRCh38
NC_000011.9:g.32625912_32625924del , CM000673.1:g.32625912_32625924del GRCh37
NC_000011.8:g.32582488_32582500del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000335185.10:c.3031-1357_3031-1345del (CCDC73) MANE Select ENSP00000335325.5:n.3031-1357_3031-1345del
ENST00000531120.6:c.*1967_*1979del (EIF3M) MANE Select ENSP00000436049.1:n.*1967_*1979del
ENST00000335185.9:c.3031-1357_3031-1345del (CCDC73) ENSP00000335325.5:n.3031-1357_3031-1345del
ENST00000528333.1:c.138-1357_138-1345del (CCDC73)
ENST00000531120.5:c.*1967_*1979del (EIF3M) ENSP00000436049.1:n.*1967_*1979del
NM_001008391.3:c.3031-1357_3031-1345del (CCDC73) NP_001008392.2:n.3031-1357_3031-1345del
XM_011519840.1:c.*1967_*1979del (EIF3M) XP_011518142.1:n.*1967_*1979del
XM_011520139.1:c.2773-1357_2773-1345del (CCDC73) XP_011518441.1:n.2773-1357_2773-1345del
NM_006360.6:c.*1967_*1979del (EIF3M) MANE Select NP_006351.2:n.*1967_*1979del
NM_001307929.2:c.*1967_*1979del (EIF3M) NP_001294858.1:n.*1967_*1979del
NM_001008391.4:c.3031-1357_3031-1345del (CCDC73) MANE Select NP_001008392.2:n.3031-1357_3031-1345del
Search 100 bp 5'
Search 100 bp 3'