Canonical Allele Identifier: CA2578752636

Gene: IFNGR1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.137206087del , CM000668.2:g.137206087del	GRCh38
NC_000006.11:g.137527224del , CM000668.1:g.137527224del	GRCh37
NC_000006.10:g.137568917del	NCBI36
NG_007394.1:g.18344del , LRG_66:g.18344del

Transcript Alleles

HGVS	Amino-acid change
ENST00000414770.6:c.343+49del	ENSP00000394230.2:n.343+49del
ENST00000458076.6:c.271+49del	ENSP00000389249.2:n.271+49del
ENST00000696693.1:c.250+49del	ENSP00000512814.1:n.250+49del
ENST00000696694.1:c.373+49del	ENSP00000512815.1:n.373+49del
ENST00000696695.1:c.373+49del	ENSP00000512816.1:n.373+49del
ENST00000696696.1:c.*272+49del	ENSP00000512817.1:n.*272+49del
ENST00000696697.1:c.319+49del	ENSP00000512818.1:n.319+49del
ENST00000696698.1:c.373+49del	ENSP00000512819.1:n.373+49del
ENST00000696699.1:c.289+49del	ENSP00000512820.1:n.289+49del
ENST00000367739.9:c.373+49del MANE Select	ENSP00000356713.5:n.373+49del
ENST00000642390.1:c.316+49del	ENSP00000496468.1:n.316+49del
ENST00000643119.1:c.493+49del	ENSP00000495934.1:n.493+49del
ENST00000644894.1:c.250+49del	ENSP00000495272.1:n.250+49del
ENST00000645045.1:c.482+49del
ENST00000645753.1:c.250+49del	ENSP00000495103.1:n.250+49del
ENST00000646036.1:c.343+49del	ENSP00000496387.1:n.343+49del
ENST00000646898.1:c.343+49del	ENSP00000494069.1:n.343+49del
ENST00000647124.1:c.250+49del	ENSP00000496549.1:n.250+49del
ENST00000367739.8:c.373+49del	ENSP00000356713.4:n.373+49del
ENST00000414770.5:c.343+49del	ENSP00000394230.1:n.343+49del
ENST00000458076.5:c.271+49del	ENSP00000389249.1:n.271+49del
ENST00000543628.5:c.373+49del	ENSP00000443282.2:n.373+49del
NM_000416.2:c.373+49del , LRG_66t1:c.373+49del	NP_000407.1:n.373+49del
XM_006715470.2:c.343+49del	XP_006715533.1:n.343+49del
XM_006715471.2:c.250+49del	XP_006715534.1:n.250+49del
XM_011535793.1:c.343+49del	XP_011534095.1:n.343+49del
XM_011535794.1:c.343+49del	XP_011534096.1:n.343+49del
NM_001363526.1:c.343+49del	NP_001350455.1:n.343+49del
NM_001363527.1:c.250+49del	NP_001350456.1:n.250+49del
XM_006715470.3:c.343+49del	XP_006715533.1:n.343+49del
XM_011535793.2:c.343+49del	XP_011534095.1:n.343+49del
NM_000416.3:c.373+49del MANE Select	NP_000407.1:n.373+49del