Canonical Allele Identifier: CA646687307

Gene: IL18RAP

Linked Data

• COSMIC: COSN8754697

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.102438227T>A , CM000664.2:g.102438227T>A	GRCh38
NC_000002.11:g.103054687T>A , CM000664.1:g.103054687T>A	GRCh37
NC_000002.10:g.102421119T>A	NCBI36
NG_011481.1:g.24434T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000687160.1:c.730+865T>A MANE Select	ENSP00000510345.1:n.730+865T>A
ENST00000264260.6:c.730+865T>A	ENSP00000264260.2:n.730+865T>A
ENST00000409369.1:c.304+865T>A	ENSP00000387201.1:n.304+865T>A
NM_003853.3:c.730+865T>A	NP_003844.1:n.730+865T>A
XM_011512087.1:c.304+865T>A	XP_011510389.1:n.304+865T>A
XM_011512088.1:c.304+865T>A	XP_011510390.1:n.304+865T>A
XM_011512089.1:c.730+865T>A	XP_011510391.1:n.730+865T>A
XR_923052.1:n.1067+865T>A
XM_011512087.2:c.304+865T>A	XP_011510389.1:n.304+865T>A
XM_011512088.2:c.304+865T>A	XP_011510390.1:n.304+865T>A
XM_024453197.1:c.730+865T>A	XP_024308965.1:n.730+865T>A
XM_024453198.1:c.730+865T>A	XP_024308966.1:n.730+865T>A
XM_024453199.1:c.730+865T>A	XP_024308967.1:n.730+865T>A
XM_024453200.1:c.730+865T>A	XP_024308968.1:n.730+865T>A
XM_024453201.1:c.730+865T>A	XP_024308969.1:n.730+865T>A
XR_001739011.2:n.1065+865T>A
NM_001393486.1:c.730+865T>A	NP_001380415.1:n.730+865T>A
NM_001393487.1:c.730+865T>A MANE Select	NP_001380416.1:n.730+865T>A
NM_001393488.1:c.304+865T>A	NP_001380417.1:n.304+865T>A
NM_001393489.1:c.304+865T>A	NP_001380418.1:n.304+865T>A
NM_003853.4:c.730+865T>A	NP_003844.1:n.730+865T>A