Canonical Allele Identifier: CA2751473535

Gene: IL18RAP

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.102419461A>C , CM000664.2:g.102419461A>C	GRCh38
NC_000002.11:g.103035921A>C , CM000664.1:g.103035921A>C	GRCh37
NC_000002.10:g.102402353A>C	NCBI36
NG_011481.1:g.5668A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264260.6:c.-337-100A>C	ENSP00000264260.2:n.-337-100A>C
ENST00000450855.1:c.-437A>C	ENSP00000389815.1:n.-437A>C
NM_003853.3:c.-337-100A>C	NP_003844.1:n.-337-100A>C
XM_011512087.1:c.-438-100A>C	XP_011510389.1:n.-438-100A>C
XM_011512087.2:c.-438-100A>C	XP_011510389.1:n.-438-100A>C
XM_024453197.1:c.-1292-100A>C	XP_024308965.1:n.-1292-100A>C
XM_024453198.1:c.-446-100A>C	XP_024308966.1:n.-446-100A>C
XM_024453199.1:c.-589-100A>C	XP_024308967.1:n.-589-100A>C
XM_024453201.1:c.-101+521A>C	XP_024308969.1:n.-101+521A>C
NM_001393486.1:c.-337-100A>C	NP_001380415.1:n.-337-100A>C
NM_001393488.1:c.-967-100A>C	NP_001380417.1:n.-967-100A>C
NM_001393489.1:c.-438-100A>C	NP_001380418.1:n.-438-100A>C
NM_003853.4:c.-337-100A>C	NP_003844.1:n.-337-100A>C