Canonical Allele Identifier: CA1280040338

Gene: IL36RN

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.113062361_113062362delinsAT , CM000664.2:g.113062361_113062362delinsAT	GRCh38
NC_000002.11:g.113819938_113819939delinsAT , CM000664.1:g.113819938_113819939delinsAT	GRCh37
NC_000002.10:g.113536409_113536410delinsAT	NCBI36
NG_031864.1:g.8724_8725delinsAT , LRG_730:g.8724_8725delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000437409.2:c.244-92_244-91delinsAT	ENSP00000409262.2:n.244-92_244-91delinsAT
ENST00000393200.7:c.244-92_244-91delinsAT MANE Select	ENSP00000376896.2:n.244-92_244-91delinsAT
ENST00000346807.7:c.244-92_244-91delinsAT	ENSP00000259212.3:n.244-92_244-91delinsAT
ENST00000393200.6:c.244-92_244-91delinsAT	ENSP00000376896.2:n.244-92_244-91delinsAT
ENST00000437409.1:c.244-92_244-91delinsAT	ENSP00000409262.1:n.244-92_244-91delinsAT
NM_012275.2:c.244-92_244-91delinsAT , LRG_730t2:c.244-92_244-91delinsAT	NP_036407.1:n.244-92_244-91delinsAT
NM_173170.1:c.244-92_244-91delinsAT , LRG_730t1:c.244-92_244-91delinsAT	NP_775262.1:n.244-92_244-91delinsAT
NM_012275.3:c.244-92_244-91delinsAT MANE Select	NP_036407.1:n.244-92_244-91delinsAT