Canonical Allele Identifier: CA1275264089

Gene: IL18RAP

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.102441479_102441480delinsTG , CM000664.2:g.102441479_102441480delinsTG	GRCh38
NC_000002.11:g.103057939_103057940delinsTG , CM000664.1:g.103057939_103057940delinsTG	GRCh37
NC_000002.10:g.102424371_102424372delinsTG	NCBI36
NG_011481.1:g.27686_27687delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000687160.1:c.796+102_796+103delinsTG MANE Select	ENSP00000510345.1:n.796+102_796+103delinsTG
ENST00000264260.6:c.796+102_796+103delinsTG	ENSP00000264260.2:n.796+102_796+103delinsTG
ENST00000409369.1:c.370+102_370+103delinsTG	ENSP00000387201.1:n.370+102_370+103delinsTG
NM_003853.3:c.796+102_796+103delinsTG	NP_003844.1:n.796+102_796+103delinsTG
XM_011512087.1:c.370+102_370+103delinsTG	XP_011510389.1:n.370+102_370+103delinsTG
XM_011512088.1:c.370+102_370+103delinsTG	XP_011510390.1:n.370+102_370+103delinsTG
XM_011512089.1:c.796+102_796+103delinsTG	XP_011510391.1:n.796+102_796+103delinsTG
XR_923052.1:n.1133+102_1133+103delinsTG
XM_011512087.2:c.370+102_370+103delinsTG	XP_011510389.1:n.370+102_370+103delinsTG
XM_011512088.2:c.370+102_370+103delinsTG	XP_011510390.1:n.370+102_370+103delinsTG
XM_024453197.1:c.796+102_796+103delinsTG	XP_024308965.1:n.796+102_796+103delinsTG
XM_024453198.1:c.796+102_796+103delinsTG	XP_024308966.1:n.796+102_796+103delinsTG
XM_024453199.1:c.796+102_796+103delinsTG	XP_024308967.1:n.796+102_796+103delinsTG
XM_024453200.1:c.796+102_796+103delinsTG	XP_024308968.1:n.796+102_796+103delinsTG
XM_024453201.1:c.796+102_796+103delinsTG	XP_024308969.1:n.796+102_796+103delinsTG
XR_001739011.2:n.1131+102_1131+103delinsTG
NM_001393486.1:c.796+102_796+103delinsTG	NP_001380415.1:n.796+102_796+103delinsTG
NM_001393487.1:c.796+102_796+103delinsTG MANE Select	NP_001380416.1:n.796+102_796+103delinsTG
NM_001393488.1:c.370+102_370+103delinsTG	NP_001380417.1:n.370+102_370+103delinsTG
NM_001393489.1:c.370+102_370+103delinsTG	NP_001380418.1:n.370+102_370+103delinsTG
NM_003853.4:c.796+102_796+103delinsTG	NP_003844.1:n.796+102_796+103delinsTG