Canonical Allele Identifier: CA1303149206

Gene: IFIH1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.162282228_162282231delinsAAGT , CM000664.2:g.162282228_162282231delinsAAGT	GRCh38
NC_000002.11:g.163138738_163138741delinsAAGT , CM000664.1:g.163138738_163138741delinsAAGT	GRCh37
NC_000002.10:g.162846984_162846987delinsAAGT	NCBI36
NG_011495.1:g.41299_41302delinsACTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697291.1:c.*903+135_*903+138delinsACTT	ENSP00000513228.1:n.*903+135_*903+138delinsACTT
ENST00000648433.1:c.1306+135_1306+138delinsACTT	ENSP00000496816.1:n.1306+135_1306+138delinsACTT
ENST00000649554.1:n.916+135_916+138delinsACTT
ENST00000649979.2:c.1306+135_1306+138delinsACTT MANE Select	ENSP00000497271.1:n.1306+135_1306+138delinsACTT
ENST00000679938.1:c.994+135_994+138delinsACTT	ENSP00000505518.1:n.994+135_994+138delinsACTT
ENST00000263642.2:c.1306+135_1306+138delinsACTT	ENSP00000263642.2:n.1306+135_1306+138delinsACTT
NM_022168.3:c.1306+135_1306+138delinsACTT	NP_071451.2:n.1306+135_1306+138delinsACTT
XM_011511628.1:c.589+135_589+138delinsACTT	XP_011509930.1:n.589+135_589+138delinsACTT
XM_011511629.1:c.1306+135_1306+138delinsACTT	XP_011509931.1:n.1306+135_1306+138delinsACTT
NM_022168.4:c.1306+135_1306+138delinsACTT MANE Select	NP_071451.2:n.1306+135_1306+138delinsACTT