Canonical Allele Identifier: CA347946921
Gene: IL18RAP HGNC NCBI

Linked Data

dbSNP Id: rs1428853287

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.102451835A>G , CM000664.2:g.102451835A>G GRCh38
NC_000002.11:g.103068295A>G , CM000664.1:g.103068295A>G GRCh37
NC_000002.10:g.102434727A>G NCBI36
NG_011481.1:g.38042A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000687160.1:c.1454A>G MANE Select ENSP00000510345.1:p.Tyr485Cys
ENST00000264260.6:c.1454A>G ENSP00000264260.2:p.Tyr485Cys
ENST00000409369.1:c.1028A>G ENSP00000387201.1:p.Tyr343Cys
NM_003853.3:c.1454A>G NP_003844.1:p.Tyr485Cys
XM_011512087.1:c.1028A>G XP_011510389.1:p.Tyr343Cys
XM_011512088.1:c.1028A>G XP_011510390.1:p.Tyr343Cys
XM_011512087.2:c.1028A>G XP_011510389.1:p.Tyr343Cys
XM_011512088.2:c.1028A>G XP_011510390.1:p.Tyr343Cys
XM_017005173.1:c.596A>G XP_016860662.1:p.Tyr199Cys
XM_024453197.1:c.1454A>G XP_024308965.1:p.Tyr485Cys
XM_024453198.1:c.1454A>G XP_024308966.1:p.Tyr485Cys
XM_024453199.1:c.1454A>G XP_024308967.1:p.Tyr485Cys
XM_024453200.1:c.1454A>G XP_024308968.1:p.Tyr485Cys
XM_024453201.1:c.1454A>G XP_024308969.1:p.Tyr485Cys
NM_001393486.1:c.1454A>G NP_001380415.1:p.Tyr485Cys
NM_001393487.1:c.1454A>G MANE Select NP_001380416.1:p.Tyr485Cys
NM_001393488.1:c.1028A>G NP_001380417.1:p.Tyr343Cys
NM_001393489.1:c.1028A>G NP_001380418.1:p.Tyr343Cys
NM_003853.4:c.1454A>G NP_003844.1:p.Tyr485Cys