Canonical Allele Identifier: CA1275266557

Gene: IL18RAP

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.102451796A= , CM000664.2:g.102451796A=	GRCh38
NC_000002.11:g.103068256A= , CM000664.1:g.103068256A=	GRCh37
NC_000002.10:g.102434688A=	NCBI36
NG_011481.1:g.38003A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000687160.1:c.1415A= MANE Select	ENSP00000510345.1:p.Lys472=
ENST00000264260.6:c.1415A=	ENSP00000264260.2:p.Lys472=
ENST00000409369.1:c.989A=	ENSP00000387201.1:p.Lys330=
NM_003853.3:c.1415A=	NP_003844.1:p.Lys472=
XM_011512087.1:c.989A=	XP_011510389.1:p.Lys330=
XM_011512088.1:c.989A=	XP_011510390.1:p.Lys330=
XM_011512087.2:c.989A=	XP_011510389.1:p.Lys330=
XM_011512088.2:c.989A=	XP_011510390.1:p.Lys330=
XM_017005173.1:c.557A=	XP_016860662.1:p.Lys186=
XM_024453197.1:c.1415A=	XP_024308965.1:p.Lys472=
XM_024453198.1:c.1415A=	XP_024308966.1:p.Lys472=
XM_024453199.1:c.1415A=	XP_024308967.1:p.Lys472=
XM_024453200.1:c.1415A=	XP_024308968.1:p.Lys472=
XM_024453201.1:c.1415A=	XP_024308969.1:p.Lys472=
NM_001393486.1:c.1415A=	NP_001380415.1:p.Lys472=
NM_001393487.1:c.1415A= MANE Select	NP_001380416.1:p.Lys472=
NM_001393488.1:c.989A=	NP_001380417.1:p.Lys330=
NM_001393489.1:c.989A=	NP_001380418.1:p.Lys330=
NM_003853.4:c.1415A=	NP_003844.1:p.Lys472=