Canonical Allele Identifier: CA1275266648

Gene: IL18RAP

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.102451868C= , CM000664.2:g.102451868C=	GRCh38
NC_000002.11:g.103068328C= , CM000664.1:g.103068328C=	GRCh37
NC_000002.10:g.102434760C=	NCBI36
NG_011481.1:g.38075C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000687160.1:c.1487C= MANE Select	ENSP00000510345.1:p.Ala496=
ENST00000264260.6:c.1487C=	ENSP00000264260.2:p.Ala496=
ENST00000409369.1:c.1061C=	ENSP00000387201.1:p.Ala354=
NM_003853.3:c.1487C=	NP_003844.1:p.Ala496=
XM_011512087.1:c.1061C=	XP_011510389.1:p.Ala354=
XM_011512088.1:c.1061C=	XP_011510390.1:p.Ala354=
XM_011512087.2:c.1061C=	XP_011510389.1:p.Ala354=
XM_011512088.2:c.1061C=	XP_011510390.1:p.Ala354=
XM_017005173.1:c.629C=	XP_016860662.1:p.Ala210=
XM_024453197.1:c.1487C=	XP_024308965.1:p.Ala496=
XM_024453198.1:c.1487C=	XP_024308966.1:p.Ala496=
XM_024453199.1:c.1487C=	XP_024308967.1:p.Ala496=
XM_024453200.1:c.1487C=	XP_024308968.1:p.Ala496=
XM_024453201.1:c.1487C=	XP_024308969.1:p.Ala496=
NM_001393486.1:c.1487C=	NP_001380415.1:p.Ala496=
NM_001393487.1:c.1487C= MANE Select	NP_001380416.1:p.Ala496=
NM_001393488.1:c.1061C=	NP_001380417.1:p.Ala354=
NM_001393489.1:c.1061C=	NP_001380418.1:p.Ala354=
NM_003853.4:c.1487C=	NP_003844.1:p.Ala496=