Canonical Allele Identifier: CA1666385240

Gene: IFNGR1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.137204354_137204355delinsTA , CM000668.2:g.137204354_137204355delinsTA	GRCh38
NC_000006.11:g.137525491_137525492delinsTA , CM000668.1:g.137525491_137525492delinsTA	GRCh37
NC_000006.10:g.137567184_137567185delinsTA	NCBI36
NG_007394.1:g.20076_20077delinsTA , LRG_66:g.20076_20077delinsTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000414770.6:c.493_494delinsTA	ENSP00000394230.2:p.Tyr165=
ENST00000458076.6:c.421_422delinsTA	ENSP00000389249.2:p.Tyr141=
ENST00000696693.1:c.400_401delinsTA	ENSP00000512814.1:p.Tyr134=
ENST00000696694.1:c.523_524delinsTA	ENSP00000512815.1:p.Tyr175=
ENST00000696695.1:c.523_524delinsTA	ENSP00000512816.1:p.Tyr175=
ENST00000696696.1:c.*422_*423delinsTA	ENSP00000512817.1:n.*422_*423delinsTA
ENST00000696697.1:c.469_470delinsTA	ENSP00000512818.1:p.Tyr157=
ENST00000696698.1:c.523_524delinsTA	ENSP00000512819.1:p.Tyr175=
ENST00000696699.1:c.439_440delinsTA	ENSP00000512820.1:p.Tyr147=
ENST00000367739.9:c.523_524delinsTA MANE Select	ENSP00000356713.5:p.Tyr175=
ENST00000642390.1:c.466_467delinsTA	ENSP00000496468.1:p.Tyr156=
ENST00000643119.1:c.643_644delinsTA	ENSP00000495934.1:n.643_644delinsTA
ENST00000644894.1:c.400_401delinsTA	ENSP00000495272.1:p.Tyr134=
ENST00000645045.1:c.632_633delinsTA
ENST00000645753.1:c.400_401delinsTA	ENSP00000495103.1:p.Tyr134=
ENST00000646036.1:c.493_494delinsTA	ENSP00000496387.1:p.Tyr165=
ENST00000646898.1:c.493_494delinsTA	ENSP00000494069.1:p.Tyr165=
ENST00000647124.1:c.400_401delinsTA	ENSP00000496549.1:p.Tyr134=
ENST00000367739.8:c.523_524delinsTA	ENSP00000356713.4:p.Tyr175=
ENST00000458076.5:c.421_422delinsTA	ENSP00000389249.1:p.Tyr141=
ENST00000543628.5:c.523_524delinsTA	ENSP00000443282.2:p.Tyr175=
NM_000416.2:c.523_524delinsTA , LRG_66t1:c.523_524delinsTA	NP_000407.1:p.Tyr175=
XM_006715470.2:c.493_494delinsTA	XP_006715533.1:p.Tyr165=
XM_006715471.2:c.400_401delinsTA	XP_006715534.1:p.Tyr134=
XM_011535793.1:c.493_494delinsTA	XP_011534095.1:p.Tyr165=
XM_011535794.1:c.493_494delinsTA	XP_011534096.1:p.Tyr165=
NM_001363526.1:c.493_494delinsTA	NP_001350455.1:p.Tyr165=
NM_001363527.1:c.400_401delinsTA	NP_001350456.1:p.Tyr134=
XM_006715470.3:c.493_494delinsTA	XP_006715533.1:p.Tyr165=
XM_011535793.2:c.493_494delinsTA	XP_011534095.1:p.Tyr165=
NM_000416.3:c.523_524delinsTA MANE Select	NP_000407.1:p.Tyr175=