Canonical Allele Identifier: CA1275266977
Gene: IL18RAP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.102452139A= , CM000664.2:g.102452139A= GRCh38
NC_000002.11:g.103068599A= , CM000664.1:g.103068599A= GRCh37
NC_000002.10:g.102435031A= NCBI36
NG_011481.1:g.38346A=

Transcript Alleles

HGVS Amino-acid change
ENST00000687160.1:c.1758A= MANE Select ENSP00000510345.1:p.Arg586=
ENST00000264260.6:c.1758A= ENSP00000264260.2:p.Arg586=
ENST00000409369.1:c.1332A= ENSP00000387201.1:p.Arg444=
NM_003853.3:c.1758A= NP_003844.1:p.Arg586=
XM_011512087.1:c.1332A= XP_011510389.1:p.Arg444=
XM_011512088.1:c.1332A= XP_011510390.1:p.Arg444=
XM_011512087.2:c.1332A= XP_011510389.1:p.Arg444=
XM_011512088.2:c.1332A= XP_011510390.1:p.Arg444=
XM_017005173.1:c.900A= XP_016860662.1:p.Arg300=
XM_024453197.1:c.1758A= XP_024308965.1:p.Arg586=
XM_024453198.1:c.1758A= XP_024308966.1:p.Arg586=
XM_024453199.1:c.1758A= XP_024308967.1:p.Arg586=
XM_024453200.1:c.1758A= XP_024308968.1:p.Arg586=
XM_024453201.1:c.1758A= XP_024308969.1:p.Arg586=
NM_001393486.1:c.1758A= NP_001380415.1:p.Arg586=
NM_001393487.1:c.1758A= MANE Select NP_001380416.1:p.Arg586=
NM_001393488.1:c.1332A= NP_001380417.1:p.Arg444=
NM_001393489.1:c.1332A= NP_001380418.1:p.Arg444=
NM_003853.4:c.1758A= NP_003844.1:p.Arg586=