Canonical Allele Identifier: CA2519345822

Gene: IL18RAP

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.102419237A>T , CM000664.2:g.102419237A>T	GRCh38
NC_000002.11:g.103035697A>T , CM000664.1:g.103035697A>T	GRCh37
NC_000002.10:g.102402129A>T	NCBI36
NG_011481.1:g.5444A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264260.6:c.-338+297A>T	ENSP00000264260.2:n.-338+297A>T
NM_003853.3:c.-338+297A>T	NP_003844.1:n.-338+297A>T
XM_011512087.1:c.-439+297A>T	XP_011510389.1:n.-439+297A>T
XM_011512087.2:c.-439+297A>T	XP_011510389.1:n.-439+297A>T
XM_024453197.1:c.-1293+297A>T	XP_024308965.1:n.-1293+297A>T
XM_024453198.1:c.-447+297A>T	XP_024308966.1:n.-447+297A>T
XM_024453199.1:c.-590+297A>T	XP_024308967.1:n.-590+297A>T
XM_024453201.1:c.-101+297A>T	XP_024308969.1:n.-101+297A>T
NM_001393486.1:c.-338+297A>T	NP_001380415.1:n.-338+297A>T
NM_001393488.1:c.-968+297A>T	NP_001380417.1:n.-968+297A>T
NM_001393489.1:c.-439+297A>T	NP_001380418.1:n.-439+297A>T
NM_003853.4:c.-338+297A>T	NP_003844.1:n.-338+297A>T