Canonical Allele Identifier: CA2611659512
Gene: IFITM5 HGNC NCBI

Linked Data

gnomAD v4: 11-299429-TG-T

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.299432del , CM000673.2:g.299432del GRCh38
NC_000011.9:g.299432del , CM000673.1:g.299432del GRCh37
NC_000011.8:g.289432del NCBI36
NG_032892.1:g.5097del

Transcript Alleles

HGVS Amino-acid Change
ENST00000382614.2:c.61del MANE Select ENSP00000372059.2:p.His21ThrfsTer17
NM_001025295.2:c.61del NP_001020466.1:p.His21ThrfsTer17
NM_001025295.3:c.61del MANE Select NP_001020466.1:p.His21ThrfsTer17