Canonical Allele Identifier: CA2751749248
Gene: IL36RN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.113062241dup , CM000664.2:g.113062241dup GRCh38
NC_000002.11:g.113819818dup , CM000664.1:g.113819818dup GRCh37
NC_000002.10:g.113536289dup NCBI36
NG_031864.1:g.8604dup , LRG_730:g.8604dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000437409.2:c.233dup ENSP00000409262.2:p.Thr79AsnfsTer?
ENST00000393200.7:c.233dup MANE Select ENSP00000376896.2:p.Thr79AsnfsTer?
ENST00000346807.7:c.233dup ENSP00000259212.3:p.Thr79AsnfsTer?
ENST00000393200.6:c.233dup ENSP00000376896.2:p.Thr79AsnfsTer?
ENST00000437409.1:c.233dup ENSP00000409262.1:p.Thr79AsnfsTer?
NM_012275.2:c.233dup , LRG_730t2:c.233dup NP_036407.1:p.Thr79AsnfsTer?
NM_173170.1:c.233dup , LRG_730t1:c.233dup NP_775262.1:p.Thr79AsnfsTer?
NM_012275.3:c.233dup MANE Select NP_036407.1:p.Thr79AsnfsTer?