Canonical Allele Identifier: CA1275254981

Gene: IL18RAP

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.102419258G= , CM000664.2:g.102419258G=	GRCh38
NC_000002.11:g.103035718G= , CM000664.1:g.103035718G=	GRCh37
NC_000002.10:g.102402150G=	NCBI36
NG_011481.1:g.5465G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000264260.6:c.-337-303G=	ENSP00000264260.2:n.-337-303G=
NM_003853.3:c.-337-303G=	NP_003844.1:n.-337-303G=
XM_011512087.1:c.-438-303G=	XP_011510389.1:n.-438-303G=
XM_011512087.2:c.-438-303G=	XP_011510389.1:n.-438-303G=
XM_024453197.1:c.-1292-303G=	XP_024308965.1:n.-1292-303G=
XM_024453198.1:c.-446-303G=	XP_024308966.1:n.-446-303G=
XM_024453199.1:c.-589-303G=	XP_024308967.1:n.-589-303G=
XM_024453201.1:c.-101+318G=	XP_024308969.1:n.-101+318G=
NM_001393486.1:c.-337-303G=	NP_001380415.1:n.-337-303G=
NM_001393488.1:c.-967-303G=	NP_001380417.1:n.-967-303G=
NM_001393489.1:c.-438-303G=	NP_001380418.1:n.-438-303G=
NM_003853.4:c.-337-303G=	NP_003844.1:n.-337-303G=