Canonical Allele Identifier: CA5773515

Gene: IFITM5

Linked Data

• dbSNP Id: rs767789172
• ExAC: 11:299420 AGGGCTGTGT / A
• gnomAD v2: 11-299420-AGGGCTGTGT-A
• gnomAD v4: 11-299420-AGGGCTGTGT-A
• MyVariant Identifiers: chr11:g.299421_299429del (hg19) ; chr11:g.299421_299429del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.299425_299433del , CM000673.2:g.299425_299433del	GRCh38
NC_000011.9:g.299425_299433del , CM000673.1:g.299425_299433del	GRCh37
NC_000011.8:g.289425_289433del	NCBI36
NG_032892.1:g.5098_5106del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382614.2:c.62_70del MANE Select	ENSP00000372059.2:p.His21_Ala23del
NM_001025295.2:c.62_70del	NP_001020466.1:p.His21_Ala23del
NM_001025295.3:c.62_70del MANE Select	NP_001020466.1:p.His21_Ala23del