Canonical Allele Identifier: CA1034379801

Gene: IL18RAP

Linked Data

• dbSNP Id: rs1681440316
• gnomAD v3: 2-102419495-CCTCTCTCTCCCCCGTTTCTCACCAAAAAGTTTTGTGGGTAAAGTTTAGTTCATTATTTCTGCCAGAGACAGCTG-C
• gnomAD v4: 2-102419495-CCTCTCTCTCCCCCGTTTCTCACCAAAAAGTTTTGTGGGTAAAGTTTAGTTCATTATTTCTGCCAGAGACAGCTG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.102419496_102419569del , CM000664.2:g.102419496_102419569del	GRCh38
NC_000002.11:g.103035956_103036029del , CM000664.1:g.103035956_103036029del	GRCh37
NC_000002.10:g.102402388_102402461del	NCBI36
NG_011481.1:g.5703_5776del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264260.6:c.-337-65_-329del
ENST00000450855.1:c.-402_-329del	ENSP00000389815.1:n.-402_-329del
NM_003853.3:c.-337-65_-329del
XM_011512087.1:c.-438-65_-430del
XM_011512087.2:c.-438-65_-430del
XM_024453197.1:c.-1292-65_-1284del
XM_024453198.1:c.-446-65_-438del
XM_024453199.1:c.-589-65_-581del
XM_024453201.1:c.-101+556_-101+629del	XP_024308969.1:n.-101+556_-101+629del
NM_001393486.1:c.-337-65_-329del
NM_001393488.1:c.-967-65_-959del
NM_001393489.1:c.-438-65_-430del
NM_003853.4:c.-337-65_-329del