Canonical Allele Identifier: CA1303149429

Gene: IFIH1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.162282675_162282676delinsGT , CM000664.2:g.162282675_162282676delinsGT	GRCh38
NC_000002.11:g.163139185_163139186delinsGT , CM000664.1:g.163139185_163139186delinsGT	GRCh37
NC_000002.10:g.162847431_162847432delinsGT	NCBI36
NG_011495.1:g.40854_40855delinsAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697291.1:c.*693-100_*693-99delinsAC	ENSP00000513228.1:n.*693-100_*693-99delinsAC
ENST00000648433.1:c.1096-100_1096-99delinsAC	ENSP00000496816.1:n.1096-100_1096-99delinsAC
ENST00000649554.1:n.706-100_706-99delinsAC
ENST00000649979.2:c.1096-100_1096-99delinsAC MANE Select	ENSP00000497271.1:n.1096-100_1096-99delinsAC
ENST00000679938.1:c.784-100_784-99delinsAC	ENSP00000505518.1:n.784-100_784-99delinsAC
ENST00000263642.2:c.1096-100_1096-99delinsAC	ENSP00000263642.2:n.1096-100_1096-99delinsAC
NM_022168.3:c.1096-100_1096-99delinsAC	NP_071451.2:n.1096-100_1096-99delinsAC
XM_011511628.1:c.379-100_379-99delinsAC	XP_011509930.1:n.379-100_379-99delinsAC
XM_011511629.1:c.1096-100_1096-99delinsAC	XP_011509931.1:n.1096-100_1096-99delinsAC
NM_022168.4:c.1096-100_1096-99delinsAC MANE Select	NP_071451.2:n.1096-100_1096-99delinsAC