Canonical Allele Identifier: CA754315572

Gene: IL18RAP

Linked Data

• dbSNP Id: rs1198540384
• gnomAD v4: 2-102441492-TAACTC-T
• MyVariant Identifiers: chr2:g.103057953_103057957del (hg19) ; chr2:g.102441493_102441497del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.102441494_102441498del , CM000664.2:g.102441494_102441498del	GRCh38
NC_000002.11:g.103057954_103057958del , CM000664.1:g.103057954_103057958del	GRCh37
NC_000002.10:g.102424386_102424390del	NCBI36
NG_011481.1:g.27701_27705del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000687160.1:c.796+117_796+121del MANE Select	ENSP00000510345.1:n.796+117_796+121del
ENST00000264260.6:c.796+117_796+121del	ENSP00000264260.2:n.796+117_796+121del
ENST00000409369.1:c.370+117_370+121del	ENSP00000387201.1:n.370+117_370+121del
NM_003853.3:c.796+117_796+121del	NP_003844.1:n.796+117_796+121del
XM_011512087.1:c.370+117_370+121del	XP_011510389.1:n.370+117_370+121del
XM_011512088.1:c.370+117_370+121del	XP_011510390.1:n.370+117_370+121del
XM_011512089.1:c.796+117_796+121del	XP_011510391.1:n.796+117_796+121del
XR_923052.1:n.1133+117_1133+121del
XM_011512087.2:c.370+117_370+121del	XP_011510389.1:n.370+117_370+121del
XM_011512088.2:c.370+117_370+121del	XP_011510390.1:n.370+117_370+121del
XM_024453197.1:c.796+117_796+121del	XP_024308965.1:n.796+117_796+121del
XM_024453198.1:c.796+117_796+121del	XP_024308966.1:n.796+117_796+121del
XM_024453199.1:c.796+117_796+121del	XP_024308967.1:n.796+117_796+121del
XM_024453200.1:c.796+117_796+121del	XP_024308968.1:n.796+117_796+121del
XM_024453201.1:c.796+117_796+121del	XP_024308969.1:n.796+117_796+121del
XR_001739011.2:n.1131+117_1131+121del
NM_001393486.1:c.796+117_796+121del	NP_001380415.1:n.796+117_796+121del
NM_001393487.1:c.796+117_796+121del MANE Select	NP_001380416.1:n.796+117_796+121del
NM_001393488.1:c.370+117_370+121del	NP_001380417.1:n.370+117_370+121del
NM_001393489.1:c.370+117_370+121del	NP_001380418.1:n.370+117_370+121del
NM_003853.4:c.796+117_796+121del	NP_003844.1:n.796+117_796+121del