Canonical Allele Identifier: CA1303148844

Gene: IFIH1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.162281577_162281578delinsCA , CM000664.2:g.162281577_162281578delinsCA	GRCh38
NC_000002.11:g.163138087_163138088delinsCA , CM000664.1:g.163138087_163138088delinsCA	GRCh37
NC_000002.10:g.162846333_162846334delinsCA	NCBI36
NG_011495.1:g.41952_41953delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697291.1:c.*904-33_*904-32delinsTG	ENSP00000513228.1:n.*904-33_*904-32delinsTG
ENST00000648433.1:c.1307-33_1307-32delinsTG	ENSP00000496816.1:n.1307-33_1307-32delinsTG
ENST00000649554.1:n.917-33_917-32delinsTG
ENST00000649979.2:c.1307-33_1307-32delinsTG MANE Select	ENSP00000497271.1:n.1307-33_1307-32delinsTG
ENST00000679938.1:c.995-33_995-32delinsTG	ENSP00000505518.1:n.995-33_995-32delinsTG
ENST00000263642.2:c.1307-33_1307-32delinsTG	ENSP00000263642.2:n.1307-33_1307-32delinsTG
NM_022168.3:c.1307-33_1307-32delinsTG	NP_071451.2:n.1307-33_1307-32delinsTG
XM_011511628.1:c.590-33_590-32delinsTG	XP_011509930.1:n.590-33_590-32delinsTG
XM_011511629.1:c.1307-33_1307-32delinsTG	XP_011509931.1:n.1307-33_1307-32delinsTG
NM_022168.4:c.1307-33_1307-32delinsTG MANE Select	NP_071451.2:n.1307-33_1307-32delinsTG