Canonical Allele Identifier: CA347947034
Gene: IL18RAP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.102451844G>C , CM000664.2:g.102451844G>C GRCh38
NC_000002.11:g.103068304G>C , CM000664.1:g.103068304G>C GRCh37
NC_000002.10:g.102434736G>C NCBI36
NG_011481.1:g.38051G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000687160.1:c.1463G>C MANE Select ENSP00000510345.1:p.Gly488Ala
ENST00000264260.6:c.1463G>C ENSP00000264260.2:p.Gly488Ala
ENST00000409369.1:c.1037G>C ENSP00000387201.1:p.Gly346Ala
NM_003853.3:c.1463G>C NP_003844.1:p.Gly488Ala
XM_011512087.1:c.1037G>C XP_011510389.1:p.Gly346Ala
XM_011512088.1:c.1037G>C XP_011510390.1:p.Gly346Ala
XM_011512087.2:c.1037G>C XP_011510389.1:p.Gly346Ala
XM_011512088.2:c.1037G>C XP_011510390.1:p.Gly346Ala
XM_017005173.1:c.605G>C XP_016860662.1:p.Gly202Ala
XM_024453197.1:c.1463G>C XP_024308965.1:p.Gly488Ala
XM_024453198.1:c.1463G>C XP_024308966.1:p.Gly488Ala
XM_024453199.1:c.1463G>C XP_024308967.1:p.Gly488Ala
XM_024453200.1:c.1463G>C XP_024308968.1:p.Gly488Ala
XM_024453201.1:c.1463G>C XP_024308969.1:p.Gly488Ala
NM_001393486.1:c.1463G>C NP_001380415.1:p.Gly488Ala
NM_001393487.1:c.1463G>C MANE Select NP_001380416.1:p.Gly488Ala
NM_001393488.1:c.1037G>C NP_001380417.1:p.Gly346Ala
NM_001393489.1:c.1037G>C NP_001380418.1:p.Gly346Ala
NM_003853.4:c.1463G>C NP_003844.1:p.Gly488Ala