Canonical Allele Identifier: CA1275264099

Gene: IL18RAP

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.102441499G= , CM000664.2:g.102441499G=	GRCh38
NC_000002.11:g.103057959G= , CM000664.1:g.103057959G=	GRCh37
NC_000002.10:g.102424391G=	NCBI36
NG_011481.1:g.27706G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000687160.1:c.796+122G= MANE Select	ENSP00000510345.1:n.796+122G=
ENST00000264260.6:c.796+122G=	ENSP00000264260.2:n.796+122G=
ENST00000409369.1:c.370+122G=	ENSP00000387201.1:n.370+122G=
NM_003853.3:c.796+122G=	NP_003844.1:n.796+122G=
XM_011512087.1:c.370+122G=	XP_011510389.1:n.370+122G=
XM_011512088.1:c.370+122G=	XP_011510390.1:n.370+122G=
XM_011512089.1:c.796+122G=	XP_011510391.1:n.796+122G=
XR_923052.1:n.1133+122G=
XM_011512087.2:c.370+122G=	XP_011510389.1:n.370+122G=
XM_011512088.2:c.370+122G=	XP_011510390.1:n.370+122G=
XM_024453197.1:c.796+122G=	XP_024308965.1:n.796+122G=
XM_024453198.1:c.796+122G=	XP_024308966.1:n.796+122G=
XM_024453199.1:c.796+122G=	XP_024308967.1:n.796+122G=
XM_024453200.1:c.796+122G=	XP_024308968.1:n.796+122G=
XM_024453201.1:c.796+122G=	XP_024308969.1:n.796+122G=
XR_001739011.2:n.1131+122G=
NM_001393486.1:c.796+122G=	NP_001380415.1:n.796+122G=
NM_001393487.1:c.796+122G= MANE Select	NP_001380416.1:n.796+122G=
NM_001393488.1:c.370+122G=	NP_001380417.1:n.370+122G=
NM_001393489.1:c.370+122G=	NP_001380418.1:n.370+122G=
NM_003853.4:c.796+122G=	NP_003844.1:n.796+122G=