Canonical Allele Identifier: CA1275266360
Gene: IL18RAP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.102451599C= , CM000664.2:g.102451599C= GRCh38
NC_000002.11:g.103068059C= , CM000664.1:g.103068059C= GRCh37
NC_000002.10:g.102434491C= NCBI36
NG_011481.1:g.37806C=

Transcript Alleles

HGVS Amino-acid change
ENST00000687160.1:c.1385-167C= MANE Select ENSP00000510345.1:n.1385-167C=
ENST00000264260.6:c.1385-167C= ENSP00000264260.2:n.1385-167C=
ENST00000409369.1:c.959-167C= ENSP00000387201.1:n.959-167C=
NM_003853.3:c.1385-167C= NP_003844.1:n.1385-167C=
XM_011512087.1:c.959-167C= XP_011510389.1:n.959-167C=
XM_011512088.1:c.959-167C= XP_011510390.1:n.959-167C=
XM_011512087.2:c.959-167C= XP_011510389.1:n.959-167C=
XM_011512088.2:c.959-167C= XP_011510390.1:n.959-167C=
XM_017005173.1:c.527-167C= XP_016860662.1:n.527-167C=
XM_024453197.1:c.1385-167C= XP_024308965.1:n.1385-167C=
XM_024453198.1:c.1385-167C= XP_024308966.1:n.1385-167C=
XM_024453199.1:c.1385-167C= XP_024308967.1:n.1385-167C=
XM_024453200.1:c.1385-167C= XP_024308968.1:n.1385-167C=
XM_024453201.1:c.1385-167C= XP_024308969.1:n.1385-167C=
NM_001393486.1:c.1385-167C= NP_001380415.1:n.1385-167C=
NM_001393487.1:c.1385-167C= MANE Select NP_001380416.1:n.1385-167C=
NM_001393488.1:c.959-167C= NP_001380417.1:n.959-167C=
NM_001393489.1:c.959-167C= NP_001380418.1:n.959-167C=
NM_003853.4:c.1385-167C= NP_003844.1:n.1385-167C=