Canonical Allele Identifier: CA1280040402
Gene: IL36RN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.113062472_113062513delinsTCTATCTTGGTGCCAAGGAATCCAAGAGCTTCACCTTCTACC , CM000664.2:g.113062472_113062513delinsTCTATCTTGGTGCCAAGGAATCCAAGAGCTTCACCTTCTACC GRCh38
NC_000002.11:g.113820049_113820090delinsTCTATCTTGGTGCCAAGGAATCCAAGAGCTTCACCTTCTACC , CM000664.1:g.113820049_113820090delinsTCTATCTTGGTGCCAAGGAATCCAAGAGCTTCACCTTCTACC GRCh37
NC_000002.10:g.113536520_113536561delinsTCTATCTTGGTGCCAAGGAATCCAAGAGCTTCACCTTCTACC NCBI36
NG_031864.1:g.8835_8876delinsTCTATCTTGGTGCCAAGGAATCCAAGAGCTTCACCTTCTACC , LRG_730:g.8835_8876delinsTCTATCTTGGTGCCAAGGAATCCAAGAGCTTCACCTTCTACC

Transcript Alleles

HGVS Amino-acid Change
ENST00000437409.2:c.263_304delinsTCTATCTTGGTGCCAAGGAATCCAAGAGCTTCACCTTCTACC ENSP00000409262.2:p.Leu88=
ENST00000393200.7:c.263_304delinsTCTATCTTGGTGCCAAGGAATCCAAGAGCTTCACCTTCTACC MANE Select ENSP00000376896.2:p.Leu88=
ENST00000346807.7:c.263_304delinsTCTATCTTGGTGCCAAGGAATCCAAGAGCTTCACCTTCTACC ENSP00000259212.3:p.Leu88=
ENST00000393200.6:c.263_304delinsTCTATCTTGGTGCCAAGGAATCCAAGAGCTTCACCTTCTACC ENSP00000376896.2:p.Leu88=
ENST00000437409.1:c.263_304delinsTCTATCTTGGTGCCAAGGAATCCAAGAGCTTCACCTTCTACC ENSP00000409262.1:p.Leu88=
NM_012275.2:c.263_304delinsTCTATCTTGGTGCCAAGGAATCCAAGAGCTTCACCTTCTACC , LRG_730t2:c.263_304delinsTCTATCTTGGTGCCAAGGAATCCAAGAGCTTCACCTTCTACC NP_036407.1:p.Leu88=
NM_173170.1:c.263_304delinsTCTATCTTGGTGCCAAGGAATCCAAGAGCTTCACCTTCTACC , LRG_730t1:c.263_304delinsTCTATCTTGGTGCCAAGGAATCCAAGAGCTTCACCTTCTACC NP_775262.1:p.Leu88=
NM_012275.3:c.263_304delinsTCTATCTTGGTGCCAAGGAATCCAAGAGCTTCACCTTCTACC MANE Select NP_036407.1:p.Leu88=