Canonical Allele Identifier: CA1275265512

Gene: IL18RAP

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.102444423_102444430delinsAATAGCCT , CM000664.2:g.102444423_102444430delinsAATAGCCT	GRCh38
NC_000002.11:g.103060883_103060890delinsAATAGCCT , CM000664.1:g.103060883_103060890delinsAATAGCCT	GRCh37
NC_000002.10:g.102427315_102427322delinsAATAGCCT	NCBI36
NG_011481.1:g.30630_30637delinsAATAGCCT

Transcript Alleles

HGVS	Amino-acid change
ENST00000687160.1:c.921-766_921-759delinsAATAGCCT MANE Select	ENSP00000510345.1:n.921-766_921-759delins...
ENST00000264260.6:c.921-766_921-759delinsAATAGCCT	ENSP00000264260.2:n.921-766_921-759delins...
ENST00000409369.1:c.495-766_495-759delinsAATAGCCT	ENSP00000387201.1:n.495-766_495-759delins...
NM_003853.3:c.921-766_921-759delinsAATAGCCT	NP_003844.1:n.921-766_921-759delinsAATAGC...
XM_011512087.1:c.495-766_495-759delinsAATAGCCT	XP_011510389.1:n.495-766_495-759delinsAAT...
XM_011512088.1:c.495-766_495-759delinsAATAGCCT	XP_011510390.1:n.495-766_495-759delinsAAT...
XR_923052.1:n.1352+331_1352+338delinsAATAGCCT
XM_011512087.2:c.495-766_495-759delinsAATAGCCT	XP_011510389.1:n.495-766_495-759delinsAAT...
XM_011512088.2:c.495-766_495-759delinsAATAGCCT	XP_011510390.1:n.495-766_495-759delinsAAT...
XM_017005173.1:c.62+331_62+338delinsAATAGCCT	XP_016860662.1:n.62+331_62+338delinsAATAG...
XM_024453197.1:c.921-766_921-759delinsAATAGCCT	XP_024308965.1:n.921-766_921-759delinsAAT...
XM_024453198.1:c.921-766_921-759delinsAATAGCCT	XP_024308966.1:n.921-766_921-759delinsAAT...
XM_024453199.1:c.921-766_921-759delinsAATAGCCT	XP_024308967.1:n.921-766_921-759delinsAAT...
XM_024453200.1:c.921-766_921-759delinsAATAGCCT	XP_024308968.1:n.921-766_921-759delinsAAT...
XM_024453201.1:c.921-766_921-759delinsAATAGCCT	XP_024308969.1:n.921-766_921-759delinsAAT...
XR_001739011.2:n.1832+331_1832+338delinsAATAGCCT
NM_001393486.1:c.921-766_921-759delinsAATAGCCT	NP_001380415.1:n.921-766_921-759delinsAAT...
NM_001393487.1:c.921-766_921-759delinsAATAGCCT MANE Select	NP_001380416.1:n.921-766_921-759delinsAAT...
NM_001393488.1:c.495-766_495-759delinsAATAGCCT	NP_001380417.1:n.495-766_495-759delinsAAT...
NM_001393489.1:c.495-766_495-759delinsAATAGCCT	NP_001380418.1:n.495-766_495-759delinsAAT...
NM_003853.4:c.921-766_921-759delinsAATAGCCT	NP_003844.1:n.921-766_921-759delinsAATAGC...