Canonical Allele Identifier: CA916610982

Gene: IL18RAP

Linked Data

• dbSNP Id: rs1558649931
• gnomAD v3: 2-102451788-CATT-C
• gnomAD v4: 2-102451788-CATT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.102451793_102451795del , CM000664.2:g.102451793_102451795del	GRCh38
NC_000002.11:g.103068253_103068255del , CM000664.1:g.103068253_103068255del	GRCh37
NC_000002.10:g.102434685_102434687del	NCBI36
NG_011481.1:g.38000_38002del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000687160.1:c.1412_1414del MANE Select	ENSP00000510345.1:p.Ile471del
ENST00000264260.6:c.1412_1414del	ENSP00000264260.2:p.Ile471del
ENST00000409369.1:c.986_988del	ENSP00000387201.1:p.Ile329del
NM_003853.3:c.1412_1414del	NP_003844.1:p.Ile471del
XM_011512087.1:c.986_988del	XP_011510389.1:p.Ile329del
XM_011512088.1:c.986_988del	XP_011510390.1:p.Ile329del
XM_011512087.2:c.986_988del	XP_011510389.1:p.Ile329del
XM_011512088.2:c.986_988del	XP_011510390.1:p.Ile329del
XM_017005173.1:c.554_556del	XP_016860662.1:p.Ile185del
XM_024453197.1:c.1412_1414del	XP_024308965.1:p.Ile471del
XM_024453198.1:c.1412_1414del	XP_024308966.1:p.Ile471del
XM_024453199.1:c.1412_1414del	XP_024308967.1:p.Ile471del
XM_024453200.1:c.1412_1414del	XP_024308968.1:p.Ile471del
XM_024453201.1:c.1412_1414del	XP_024308969.1:p.Ile471del
NM_001393486.1:c.1412_1414del	NP_001380415.1:p.Ile471del
NM_001393487.1:c.1412_1414del MANE Select	NP_001380416.1:p.Ile471del
NM_001393488.1:c.986_988del	NP_001380417.1:p.Ile329del
NM_001393489.1:c.986_988del	NP_001380418.1:p.Ile329del
NM_003853.4:c.1412_1414del	NP_003844.1:p.Ile471del