Canonical Allele Identifier: CA1303151896
Community Standard Title: NM_022168.4(IFIH1):c.1009A= (p.Arg337=)
Gene: IFIH1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.162288221T= , CM000664.2:g.162288221T= GRCh38
NC_000002.11:g.163144731T= , CM000664.1:g.163144731T= GRCh37
NC_000002.10:g.162852977T= NCBI36
NG_011495.1:g.35309A=

Transcript Alleles

HGVS Amino-acid Change
NM_022168.4:c.1009A= MANE Select NP_071451.2:p.Arg337=
ENST00000649979.2:c.1009A= MANE Select ENSP00000497271.1:p.Arg337=
NM_022168.3:c.1009A= NP_071451.2:p.Arg337=
ENST00000263642.2:c.1009A= ENSP00000263642.2:p.Arg337=
ENST00000648433.1:c.1009A= ENSP00000496816.1:p.Arg337=
ENST00000649554.1:n.619A=
ENST00000679938.1:c.697A= ENSP00000505518.1:p.Arg233=
ENST00000697291.1:c.*606A= ENSP00000513228.1:n.*606A=
XM_011511628.1:c.292A= XP_011509930.1:p.Arg98=
XM_011511629.1:c.1009A= XP_011509931.1:p.Arg337=