Canonical Allele Identifier: CA1303149251
Gene: IFIH1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.162282302_162282303delinsTA , CM000664.2:g.162282302_162282303delinsTA GRCh38
NC_000002.11:g.163138812_163138813delinsTA , CM000664.1:g.163138812_163138813delinsTA GRCh37
NC_000002.10:g.162847058_162847059delinsTA NCBI36
NG_011495.1:g.41227_41228delinsTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000697291.1:c.*903+63_*903+64delinsTA ENSP00000513228.1:n.*903+63_*903+64delinsTA
ENST00000648433.1:c.1306+63_1306+64delinsTA ENSP00000496816.1:n.1306+63_1306+64delinsTA
ENST00000649554.1:n.916+63_916+64delinsTA
ENST00000649979.2:c.1306+63_1306+64delinsTA MANE Select ENSP00000497271.1:n.1306+63_1306+64delinsTA
ENST00000679938.1:c.994+63_994+64delinsTA ENSP00000505518.1:n.994+63_994+64delinsTA
ENST00000263642.2:c.1306+63_1306+64delinsTA ENSP00000263642.2:n.1306+63_1306+64delinsTA
NM_022168.3:c.1306+63_1306+64delinsTA NP_071451.2:n.1306+63_1306+64delinsTA
XM_011511628.1:c.589+63_589+64delinsTA XP_011509930.1:n.589+63_589+64delinsTA
XM_011511629.1:c.1306+63_1306+64delinsTA XP_011509931.1:n.1306+63_1306+64delinsTA
NM_022168.4:c.1306+63_1306+64delinsTA MANE Select NP_071451.2:n.1306+63_1306+64delinsTA