Canonical Allele Identifier: CA1275266526

Gene: IL18RAP

Linked Data

• dbSNP Id: rs1683781563

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.102451765_102451780del , CM000664.2:g.102451765_102451780del	GRCh38
NC_000002.11:g.103068225_103068240del , CM000664.1:g.103068225_103068240del	GRCh37
NC_000002.10:g.102434657_102434672del	NCBI36
NG_011481.1:g.37972_37987del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000687160.1:c.1385-1_1399del
ENST00000264260.6:c.1385-1_1399del
ENST00000409369.1:c.959-1_973del
NM_003853.3:c.1385-1_1399del
XM_011512087.1:c.959-1_973del
XM_011512088.1:c.959-1_973del
XM_011512087.2:c.959-1_973del
XM_011512088.2:c.959-1_973del
XM_017005173.1:c.527-1_541del
XM_024453197.1:c.1385-1_1399del
XM_024453198.1:c.1385-1_1399del
XM_024453199.1:c.1385-1_1399del
XM_024453200.1:c.1385-1_1399del
XM_024453201.1:c.1385-1_1399del
NM_001393486.1:c.1385-1_1399del
NM_001393487.1:c.1385-1_1399del
NM_001393488.1:c.959-1_973del
NM_001393489.1:c.959-1_973del
NM_003853.4:c.1385-1_1399del