Canonical Allele Identifier: CA1280040407

Gene: IL36RN

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.113062476_113062513delinsTCTTGGTGCCAAGGAATCCAAGAGCTTCACCTTCTACC , CM000664.2:g.113062476_113062513delinsTCTTGGTGCCAAGGAATCCAAGAGCTTCACCTTCTACC	GRCh38
NC_000002.11:g.113820053_113820090delinsTCTTGGTGCCAAGGAATCCAAGAGCTTCACCTTCTACC , CM000664.1:g.113820053_113820090delinsTCTTGGTGCCAAGGAATCCAAGAGCTTCACCTTCTACC	GRCh37
NC_000002.10:g.113536524_113536561delinsTCTTGGTGCCAAGGAATCCAAGAGCTTCACCTTCTACC	NCBI36
NG_031864.1:g.8839_8876delinsTCTTGGTGCCAAGGAATCCAAGAGCTTCACCTTCTACC , LRG_730:g.8839_8876delinsTCTTGGTGCCAAGGAATCCAAGAGCTTCACCTTCTACC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000437409.2:c.267_304delinsTCTTGGTGCCAAGGAATCCAAGAGCTTCACCTTCTACC	ENSP00000409262.2:p.Tyr89=
ENST00000393200.7:c.267_304delinsTCTTGGTGCCAAGGAATCCAAGAGCTTCACCTTCTACC MANE Select	ENSP00000376896.2:p.Tyr89=
ENST00000346807.7:c.267_304delinsTCTTGGTGCCAAGGAATCCAAGAGCTTCACCTTCTACC	ENSP00000259212.3:p.Tyr89=
ENST00000393200.6:c.267_304delinsTCTTGGTGCCAAGGAATCCAAGAGCTTCACCTTCTACC	ENSP00000376896.2:p.Tyr89=
ENST00000437409.1:c.267_304delinsTCTTGGTGCCAAGGAATCCAAGAGCTTCACCTTCTACC	ENSP00000409262.1:p.Tyr89=
NM_012275.2:c.267_304delinsTCTTGGTGCCAAGGAATCCAAGAGCTTCACCTTCTACC , LRG_730t2:c.267_304delinsTCTTGGTGCCAAGGAATCCAAGAGCTTCACCTTCTACC	NP_036407.1:p.Tyr89=
NM_173170.1:c.267_304delinsTCTTGGTGCCAAGGAATCCAAGAGCTTCACCTTCTACC , LRG_730t1:c.267_304delinsTCTTGGTGCCAAGGAATCCAAGAGCTTCACCTTCTACC	NP_775262.1:p.Tyr89=
NM_012275.3:c.267_304delinsTCTTGGTGCCAAGGAATCCAAGAGCTTCACCTTCTACC MANE Select	NP_036407.1:p.Tyr89=