Canonical Allele Identifier: CA1666385208

Gene: IFNGR1

Linked Data

• dbSNP Id: rs1779371752
• gnomAD v4: 6-137204275-GAAC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.137204279_137204281del , CM000668.2:g.137204279_137204281del	GRCh38
NC_000006.11:g.137525416_137525418del , CM000668.1:g.137525416_137525418del	GRCh37
NC_000006.10:g.137567109_137567111del	NCBI36
NG_007394.1:g.20153_20155del , LRG_66:g.20153_20155del

Transcript Alleles

HGVS	Amino-acid change
ENST00000414770.6:c.516+54_516+56del	ENSP00000394230.2:n.516+54_516+56del
ENST00000458076.6:c.444+54_444+56del	ENSP00000389249.2:n.444+54_444+56del
ENST00000696693.1:c.423+54_423+56del	ENSP00000512814.1:n.423+54_423+56del
ENST00000696694.1:c.546+54_546+56del	ENSP00000512815.1:n.546+54_546+56del
ENST00000696695.1:c.546+54_546+56del	ENSP00000512816.1:n.546+54_546+56del
ENST00000696696.1:c.*445+54_*445+56del	ENSP00000512817.1:n.*445+54_*445+56del
ENST00000696697.1:c.492+54_492+56del	ENSP00000512818.1:n.492+54_492+56del
ENST00000696698.1:c.546+54_546+56del	ENSP00000512819.1:n.546+54_546+56del
ENST00000696699.1:c.462+54_462+56del	ENSP00000512820.1:n.462+54_462+56del
ENST00000367739.9:c.546+54_546+56del MANE Select	ENSP00000356713.5:n.546+54_546+56del
ENST00000642390.1:c.489+54_489+56del	ENSP00000496468.1:n.489+54_489+56del
ENST00000643119.1:c.666+54_666+56del	ENSP00000495934.1:n.666+54_666+56del
ENST00000644894.1:c.423+54_423+56del	ENSP00000495272.1:n.423+54_423+56del
ENST00000645045.1:c.655+54_655+56del
ENST00000645753.1:c.423+54_423+56del	ENSP00000495103.1:n.423+54_423+56del
ENST00000646036.1:c.516+54_516+56del	ENSP00000496387.1:n.516+54_516+56del
ENST00000646898.1:c.516+54_516+56del	ENSP00000494069.1:n.516+54_516+56del
ENST00000647124.1:c.423+54_423+56del	ENSP00000496549.1:n.423+54_423+56del
ENST00000367739.8:c.546+54_546+56del	ENSP00000356713.4:n.546+54_546+56del
ENST00000458076.5:c.444+54_444+56del	ENSP00000389249.1:n.444+54_444+56del
ENST00000543628.5:c.546+54_546+56del	ENSP00000443282.2:n.546+54_546+56del
NM_000416.2:c.546+54_546+56del , LRG_66t1:c.546+54_546+56del	NP_000407.1:n.546+54_546+56del
XM_006715470.2:c.516+54_516+56del	XP_006715533.1:n.516+54_516+56del
XM_006715471.2:c.423+54_423+56del	XP_006715534.1:n.423+54_423+56del
XM_011535793.1:c.516+54_516+56del	XP_011534095.1:n.516+54_516+56del
XM_011535794.1:c.516+54_516+56del	XP_011534096.1:n.516+54_516+56del
NM_001363526.1:c.516+54_516+56del	NP_001350455.1:n.516+54_516+56del
NM_001363527.1:c.423+54_423+56del	NP_001350456.1:n.423+54_423+56del
XM_006715470.3:c.516+54_516+56del	XP_006715533.1:n.516+54_516+56del
XM_011535793.2:c.516+54_516+56del	XP_011534095.1:n.516+54_516+56del
NM_000416.3:c.546+54_546+56del MANE Select	NP_000407.1:n.546+54_546+56del