Canonical Allele Identifier: CA347948585

Gene: IL18RAP

Linked Data

• MyVariant Identifiers: chr2:g.103068529A>C (hg19) ; chr2:g.102452069A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.102452069A>C , CM000664.2:g.102452069A>C	GRCh38
NC_000002.11:g.103068529A>C , CM000664.1:g.103068529A>C	GRCh37
NC_000002.10:g.102434961A>C	NCBI36
NG_011481.1:g.38276A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000687160.1:c.1688A>C MANE Select	ENSP00000510345.1:p.Asn563Thr
ENST00000264260.6:c.1688A>C	ENSP00000264260.2:p.Asn563Thr
ENST00000409369.1:c.1262A>C	ENSP00000387201.1:p.Asn421Thr
NM_003853.3:c.1688A>C	NP_003844.1:p.Asn563Thr
XM_011512087.1:c.1262A>C	XP_011510389.1:p.Asn421Thr
XM_011512088.1:c.1262A>C	XP_011510390.1:p.Asn421Thr
XM_011512087.2:c.1262A>C	XP_011510389.1:p.Asn421Thr
XM_011512088.2:c.1262A>C	XP_011510390.1:p.Asn421Thr
XM_017005173.1:c.830A>C	XP_016860662.1:p.Asn277Thr
XM_024453197.1:c.1688A>C	XP_024308965.1:p.Asn563Thr
XM_024453198.1:c.1688A>C	XP_024308966.1:p.Asn563Thr
XM_024453199.1:c.1688A>C	XP_024308967.1:p.Asn563Thr
XM_024453200.1:c.1688A>C	XP_024308968.1:p.Asn563Thr
XM_024453201.1:c.1688A>C	XP_024308969.1:p.Asn563Thr
NM_001393486.1:c.1688A>C	NP_001380415.1:p.Asn563Thr
NM_001393487.1:c.1688A>C MANE Select	NP_001380416.1:p.Asn563Thr
NM_001393488.1:c.1262A>C	NP_001380417.1:p.Asn421Thr
NM_001393489.1:c.1262A>C	NP_001380418.1:p.Asn421Thr
NM_003853.4:c.1688A>C	NP_003844.1:p.Asn563Thr