Canonical Allele Identifier: CA2535450416

Gene: IFIH1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.162281591_162281592insACAAAGAAG , CM000664.2:g.162281591_162281592insACAAAGAAG	GRCh38
NC_000002.11:g.163138101_163138102insACAAAGAAG , CM000664.1:g.163138101_163138102insACAAAGAAG	GRCh37
NC_000002.10:g.162846347_162846348insACAAAGAAG	NCBI36
NG_011495.1:g.41938_41939insCTTCTTTGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697291.1:c.*904-47_*904-46insCTTCTTTGT	ENSP00000513228.1:n.*904-47_*904-46insCTTCTTTGT
ENST00000648433.1:c.1307-47_1307-46insCTTCTTTGT	ENSP00000496816.1:n.1307-47_1307-46insCTTCTTTGT
ENST00000649554.1:n.917-47_917-46insCTTCTTTGT
ENST00000649979.2:c.1307-47_1307-46insCTTCTTTGT MANE Select	ENSP00000497271.1:n.1307-47_1307-46insCTTCTTTGT
ENST00000679938.1:c.995-47_995-46insCTTCTTTGT	ENSP00000505518.1:n.995-47_995-46insCTTCTTTGT
ENST00000263642.2:c.1307-47_1307-46insCTTCTTTGT	ENSP00000263642.2:n.1307-47_1307-46insCTTCTTTGT
NM_022168.3:c.1307-47_1307-46insCTTCTTTGT	NP_071451.2:n.1307-47_1307-46insCTTCTTTGT
XM_011511628.1:c.590-47_590-46insCTTCTTTGT	XP_011509930.1:n.590-47_590-46insCTTCTTTGT
XM_011511629.1:c.1307-47_1307-46insCTTCTTTGT	XP_011509931.1:n.1307-47_1307-46insCTTCTTTGT
NM_022168.4:c.1307-47_1307-46insCTTCTTTGT MANE Select	NP_071451.2:n.1307-47_1307-46insCTTCTTTGT