Canonical Allele Identifier: CA379091975

Gene: IFITM10

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.1748061C>T , CM000673.2:g.1748061C>T	GRCh38
NC_000011.9:g.1769291C>T , CM000673.1:g.1769291C>T	GRCh37
NC_000011.8:g.1725867C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340134.5:c.143G>A MANE Select	ENSP00000344430.4:p.Gly48Asp
ENST00000427721.3:c.693G>A
ENST00000636397.1:c.1130G>A	ENSP00000489910.1:p.Gly377Asp
ENST00000636579.1:c.72+5742G>A	ENSP00000490489.1:n.72+5742G>A
ENST00000636615.1:c.1130G>A	ENSP00000490014.1:p.Gly377Asp
ENST00000340134.4:c.143G>A	ENSP00000344430.4:p.Gly48Asp
ENST00000382123.1:c.255G>A	ENSP00000371557.1:p.Arg85=
ENST00000427721.2:c.530G>A	ENSP00000415840.2:p.Gly177Asp
ENST00000482459.1:n.1042G>A
ENST00000486852.1:n.238G>A
NM_001170820.3:c.143G>A	NP_001164291.2:p.Gly48Asp
NM_001170820.4:c.143G>A MANE Select	NP_001164291.2:p.Gly48Asp