Canonical Allele Identifier: CA2660747729
Gene: IL1A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.112782622del , CM000664.2:g.112782622del GRCh38
NC_000002.11:g.113540199del , CM000664.1:g.113540199del GRCh37
NC_000002.10:g.113256670del NCBI36
NG_008850.1:g.7776del

Transcript Alleles

HGVS Amino-acid Change
ENST00000263339.4:c.96+97del MANE Select ENSP00000263339.3:n.96+97del
ENST00000263339.3:c.96+97del ENSP00000263339.3:n.96+97del
NM_000575.3:c.96+97del NP_000566.3:n.96+97del
NM_000575.4:c.96+97del NP_000566.3:n.96+97del
NM_000575.5:c.96+97del MANE Select NP_000566.3:n.96+97del
NM_001371554.1:c.96+97del NP_001358483.1:n.96+97del