Canonical Allele Identifier: CA1303162511
Community Standard Title: NM_022168.4(IFIH1):c.505A= (p.Lys169=)
Gene: IFIH1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.162310882T= , CM000664.2:g.162310882T= GRCh38
NC_000002.11:g.163167392T= , CM000664.1:g.163167392T= GRCh37
NC_000002.10:g.162875638T= NCBI36
NG_011495.1:g.12648A=

Transcript Alleles

HGVS Amino-acid Change
NM_022168.4:c.505A= MANE Select NP_071451.2:p.Lys169=
ENST00000649979.2:c.505A= MANE Select ENSP00000497271.1:p.Lys169=
NM_022168.3:c.505A= NP_071451.2:p.Lys169=
ENST00000263642.2:c.505A= ENSP00000263642.2:p.Lys169=
ENST00000421365.2:c.505A= ENSP00000408450.2:p.Lys169=
ENST00000648433.1:c.505A= ENSP00000496816.1:p.Lys169=
ENST00000649554.1:n.115A=
ENST00000679938.1:c.340A= ENSP00000505518.1:p.Lys114=
ENST00000697291.1:c.*102A= ENSP00000513228.1:n.*102A=
XM_011511629.1:c.505A= XP_011509931.1:p.Lys169=