Canonical Allele Identifier: CA597017740

Gene: IFITM5

Linked Data

• dbSNP Id: rs1323254942
• gnomAD v2: 11-299424-C-CTG
• gnomAD v3: 11-299424-C-CTG
• gnomAD v4: 11-299424-C-CTG
• MyVariant Identifiers: chr11:g.299424_299425insTG (hg19) ; chr11:g.299424_299425insTG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.299429_299430dup , CM000673.2:g.299429_299430dup	GRCh38
NC_000011.9:g.299429_299430dup , CM000673.1:g.299429_299430dup	GRCh37
NC_000011.8:g.289429_289430dup	NCBI36
NG_032892.1:g.5101_5102dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382614.2:c.65_66dup MANE Select	ENSP00000372059.2:p.Ala23GlnfsTer16
NM_001025295.2:c.65_66dup	NP_001020466.1:p.Ala23GlnfsTer16
NM_001025295.3:c.65_66dup MANE Select	NP_001020466.1:p.Ala23GlnfsTer16