Canonical Allele Identifier: CA2661689081

Gene: IFIH1

Linked Data

• gnomAD v4: 2-162282219-TCCTCCAGGAAGTAGAAGGA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.162282220_162282238del , CM000664.2:g.162282220_162282238del	GRCh38
NC_000002.11:g.163138730_163138748del , CM000664.1:g.163138730_163138748del	GRCh37
NC_000002.10:g.162846976_162846994del	NCBI36
NG_011495.1:g.41292_41310del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697291.1:c.*903+128_*903+146del	ENSP00000513228.1:n.*903+128_*903+146del
ENST00000648433.1:c.1306+128_1306+146del	ENSP00000496816.1:n.1306+128_1306+146del
ENST00000649554.1:n.916+128_916+146del
ENST00000649979.2:c.1306+128_1306+146del MANE Select	ENSP00000497271.1:n.1306+128_1306+146del
ENST00000679938.1:c.994+128_994+146del	ENSP00000505518.1:n.994+128_994+146del
ENST00000263642.2:c.1306+128_1306+146del	ENSP00000263642.2:n.1306+128_1306+146del
NM_022168.3:c.1306+128_1306+146del	NP_071451.2:n.1306+128_1306+146del
XM_011511628.1:c.589+128_589+146del	XP_011509930.1:n.589+128_589+146del
XM_011511629.1:c.1306+128_1306+146del	XP_011509931.1:n.1306+128_1306+146del
NM_022168.4:c.1306+128_1306+146del MANE Select	NP_071451.2:n.1306+128_1306+146del