Canonical Allele Identifier: CA1275262670

Gene: IL18RAP

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.102438153_102438157delinsCTGTT , CM000664.2:g.102438153_102438157delinsCTGTT	GRCh38
NC_000002.11:g.103054613_103054617delinsCTGTT , CM000664.1:g.103054613_103054617delinsCTGTT	GRCh37
NC_000002.10:g.102421045_102421049delinsCTGTT	NCBI36
NG_011481.1:g.24360_24364delinsCTGTT

Transcript Alleles

HGVS	Amino-acid change
ENST00000687160.1:c.730+791_730+795delinsCTGTT MANE Select	ENSP00000510345.1:n.730+791_730+795delinsCTGTT
ENST00000264260.6:c.730+791_730+795delinsCTGTT	ENSP00000264260.2:n.730+791_730+795delinsCTGTT
ENST00000409369.1:c.304+791_304+795delinsCTGTT	ENSP00000387201.1:n.304+791_304+795delinsCTGTT
NM_003853.3:c.730+791_730+795delinsCTGTT	NP_003844.1:n.730+791_730+795delinsCTGTT
XM_011512087.1:c.304+791_304+795delinsCTGTT	XP_011510389.1:n.304+791_304+795delinsCTGTT
XM_011512088.1:c.304+791_304+795delinsCTGTT	XP_011510390.1:n.304+791_304+795delinsCTGTT
XM_011512089.1:c.730+791_730+795delinsCTGTT	XP_011510391.1:n.730+791_730+795delinsCTGTT
XR_923052.1:n.1067+791_1067+795delinsCTGTT
XM_011512087.2:c.304+791_304+795delinsCTGTT	XP_011510389.1:n.304+791_304+795delinsCTGTT
XM_011512088.2:c.304+791_304+795delinsCTGTT	XP_011510390.1:n.304+791_304+795delinsCTGTT
XM_024453197.1:c.730+791_730+795delinsCTGTT	XP_024308965.1:n.730+791_730+795delinsCTGTT
XM_024453198.1:c.730+791_730+795delinsCTGTT	XP_024308966.1:n.730+791_730+795delinsCTGTT
XM_024453199.1:c.730+791_730+795delinsCTGTT	XP_024308967.1:n.730+791_730+795delinsCTGTT
XM_024453200.1:c.730+791_730+795delinsCTGTT	XP_024308968.1:n.730+791_730+795delinsCTGTT
XM_024453201.1:c.730+791_730+795delinsCTGTT	XP_024308969.1:n.730+791_730+795delinsCTGTT
XR_001739011.2:n.1065+791_1065+795delinsCTGTT
NM_001393486.1:c.730+791_730+795delinsCTGTT	NP_001380415.1:n.730+791_730+795delinsCTGTT
NM_001393487.1:c.730+791_730+795delinsCTGTT MANE Select	NP_001380416.1:n.730+791_730+795delinsCTGTT
NM_001393488.1:c.304+791_304+795delinsCTGTT	NP_001380417.1:n.304+791_304+795delinsCTGTT
NM_001393489.1:c.304+791_304+795delinsCTGTT	NP_001380418.1:n.304+791_304+795delinsCTGTT
NM_003853.4:c.730+791_730+795delinsCTGTT	NP_003844.1:n.730+791_730+795delinsCTGTT