Canonical Allele Identifier: CA1810676
Gene: IL18RAP HGNC NCBI

Linked Data

dbSNP Id: rs754276440

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.102452084C>T , CM000664.2:g.102452084C>T GRCh38
NC_000002.11:g.103068544C>T , CM000664.1:g.103068544C>T GRCh37
NC_000002.10:g.102434976C>T NCBI36
NG_011481.1:g.38291C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000687160.1:c.1703C>T MANE Select ENSP00000510345.1:p.Thr568Met
ENST00000264260.6:c.1703C>T ENSP00000264260.2:p.Thr568Met
ENST00000409369.1:c.1277C>T ENSP00000387201.1:p.Thr426Met
NM_003853.3:c.1703C>T NP_003844.1:p.Thr568Met
XM_011512087.1:c.1277C>T XP_011510389.1:p.Thr426Met
XM_011512088.1:c.1277C>T XP_011510390.1:p.Thr426Met
XM_011512087.2:c.1277C>T XP_011510389.1:p.Thr426Met
XM_011512088.2:c.1277C>T XP_011510390.1:p.Thr426Met
XM_017005173.1:c.845C>T XP_016860662.1:p.Thr282Met
XM_024453197.1:c.1703C>T XP_024308965.1:p.Thr568Met
XM_024453198.1:c.1703C>T XP_024308966.1:p.Thr568Met
XM_024453199.1:c.1703C>T XP_024308967.1:p.Thr568Met
XM_024453200.1:c.1703C>T XP_024308968.1:p.Thr568Met
XM_024453201.1:c.1703C>T XP_024308969.1:p.Thr568Met
NM_001393486.1:c.1703C>T NP_001380415.1:p.Thr568Met
NM_001393487.1:c.1703C>T MANE Select NP_001380416.1:p.Thr568Met
NM_001393488.1:c.1277C>T NP_001380417.1:p.Thr426Met
NM_001393489.1:c.1277C>T NP_001380418.1:p.Thr426Met
NM_003853.4:c.1703C>T NP_003844.1:p.Thr568Met