Canonical Allele Identifier: CA4018811

Gene: IFNGR1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.137198400C>T , CM000668.2:g.137198400C>T	GRCh38
NC_000006.11:g.137519537C>T , CM000668.1:g.137519537C>T	GRCh37
NC_000006.10:g.137561230C>T	NCBI36
NG_007394.1:g.26031G>A , LRG_66:g.26031G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_000416.3:c.1101G>A MANE Select	NP_000407.1:p.Pro367=
ENST00000367739.9:c.1101G>A MANE Select	ENSP00000356713.5:p.Pro367=
NM_000416.2:c.1101G>A , LRG_66t1:c.1101G>A	NP_000407.1:p.Pro367=
NM_001363526.1:c.1071G>A	NP_001350455.1:p.Pro357=
NM_001363527.1:c.978G>A	NP_001350456.1:p.Pro326=
ENST00000367739.8:c.1101G>A	ENSP00000356713.4:p.Pro367=
ENST00000414770.6:c.1071G>A	ENSP00000394230.2:p.Pro357=
ENST00000458076.6:c.999G>A	ENSP00000389249.2:p.Pro333=
ENST00000543628.5:c.*272G>A	ENSP00000443282.2:n.*272G>A
ENST00000642390.1:c.1044G>A	ENSP00000496468.1:p.Pro348=
ENST00000643119.1:c.1221G>A	ENSP00000495934.1:n.1221G>A
ENST00000644894.1:c.978G>A	ENSP00000495272.1:p.Pro326=
ENST00000645045.1:c.1210G>A
ENST00000645753.1:c.978G>A	ENSP00000495103.1:p.Pro326=
ENST00000646036.1:c.1071G>A	ENSP00000496387.1:p.Pro357=
ENST00000646898.1:c.1071G>A	ENSP00000494069.1:p.Pro357=
ENST00000647124.1:c.978G>A	ENSP00000496549.1:p.Pro326=
ENST00000696693.1:c.978G>A	ENSP00000512814.1:p.Pro326=
ENST00000696694.1:c.*199G>A	ENSP00000512815.1:n.*199G>A
ENST00000696695.1:c.939G>A	ENSP00000512816.1:p.Pro313=
ENST00000696696.1:c.*1000G>A	ENSP00000512817.1:n.*1000G>A
ENST00000696697.1:c.1047G>A	ENSP00000512818.1:p.Pro349=
XM_006715470.2:c.1071G>A	XP_006715533.1:p.Pro357=
XM_006715470.3:c.1071G>A	XP_006715533.1:p.Pro357=
XM_006715471.2:c.978G>A	XP_006715534.1:p.Pro326=
XM_011535793.1:c.1071G>A	XP_011534095.1:p.Pro357=
XM_011535793.2:c.1071G>A	XP_011534095.1:p.Pro357=
XM_011535794.1:c.1071G>A	XP_011534096.1:p.Pro357=