Canonical Allele Identifier: CA2660480988

Gene: IL18RAP

Linked Data

• gnomAD v4: 2-102452225-ATGT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.102452228_102452230del , CM000664.2:g.102452228_102452230del	GRCh38
NC_000002.11:g.103068688_103068690del , CM000664.1:g.103068688_103068690del	GRCh37
NC_000002.10:g.102435120_102435122del	NCBI36
NG_011481.1:g.38435_38437del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000687160.1:c.*47_*49del MANE Select	ENSP00000510345.1:n.*47_*49del
ENST00000264260.6:c.*47_*49del	ENSP00000264260.2:n.*47_*49del
ENST00000409369.1:c.*47_*49del	ENSP00000387201.1:n.*47_*49del
NM_003853.3:c.*47_*49del	NP_003844.1:n.*47_*49del
XM_011512087.1:c.*47_*49del	XP_011510389.1:n.*47_*49del
XM_011512088.1:c.*47_*49del	XP_011510390.1:n.*47_*49del
XM_011512087.2:c.*47_*49del	XP_011510389.1:n.*47_*49del
XM_011512088.2:c.*47_*49del	XP_011510390.1:n.*47_*49del
XM_017005173.1:c.*47_*49del	XP_016860662.1:n.*47_*49del
XM_024453197.1:c.*47_*49del	XP_024308965.1:n.*47_*49del
XM_024453198.1:c.*47_*49del	XP_024308966.1:n.*47_*49del
XM_024453199.1:c.*47_*49del	XP_024308967.1:n.*47_*49del
XM_024453200.1:c.*47_*49del	XP_024308968.1:n.*47_*49del
XM_024453201.1:c.*47_*49del	XP_024308969.1:n.*47_*49del
NM_001393486.1:c.*47_*49del	NP_001380415.1:n.*47_*49del
NM_001393487.1:c.*47_*49del MANE Select	NP_001380416.1:n.*47_*49del
NM_001393488.1:c.*47_*49del	NP_001380417.1:n.*47_*49del
NM_001393489.1:c.*47_*49del	NP_001380418.1:n.*47_*49del
NM_003853.4:c.*47_*49del	NP_003844.1:n.*47_*49del