Canonical Allele Identifier: CA948825082
Gene: IL22 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.68249885_68249888del , CM000674.2:g.68249885_68249888del GRCh38
NC_000012.11:g.68643665_68643668del , CM000674.1:g.68643665_68643668del GRCh37
NC_000012.10:g.66929932_66929935del NCBI36
NG_060763.1:g.8717_8720del

Transcript Alleles

HGVS Amino-acid Change
ENST00000328087.6:c.463-1012_463-1009del ENSP00000329384.4:n.463-1012_463-1009del
ENST00000538666.6:c.463-1012_463-1009del MANE Select ENSP00000442424.1:n.463-1012_463-1009del
ENST00000328087.5:c.463-1012_463-1009del ENSP00000329384.4:n.463-1012_463-1009del
ENST00000538666.5:c.463-1012_463-1009del ENSP00000442424.1:n.463-1012_463-1009del
NM_020525.4:c.463-1012_463-1009del NP_065386.1:n.463-1012_463-1009del
XR_945055.1:n.265-14773_265-14770del
NM_020525.5:c.463-1012_463-1009del MANE Select NP_065386.1:n.463-1012_463-1009del
XR_002957418.1:n.281-14773_281-14770del