Canonical Allele Identifier: CA2043864975
Gene: IL22 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.68249950_68249951delinsTC , CM000674.2:g.68249950_68249951delinsTC GRCh38
NC_000012.11:g.68643730_68643731delinsTC , CM000674.1:g.68643730_68643731delinsTC GRCh37
NC_000012.10:g.66929997_66929998delinsTC NCBI36
NG_060763.1:g.8654_8655delinsGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000328087.6:c.463-1075_463-1074delinsGA ENSP00000329384.4:n.463-1075_463-1074delinsGA
ENST00000538666.6:c.463-1075_463-1074delinsGA MANE Select ENSP00000442424.1:n.463-1075_463-1074delinsGA
ENST00000328087.5:c.463-1075_463-1074delinsGA ENSP00000329384.4:n.463-1075_463-1074delinsGA
ENST00000538666.5:c.463-1075_463-1074delinsGA ENSP00000442424.1:n.463-1075_463-1074delinsGA
NM_020525.4:c.463-1075_463-1074delinsGA NP_065386.1:n.463-1075_463-1074delinsGA
XR_945055.1:n.265-14708_265-14707delinsTC
NM_020525.5:c.463-1075_463-1074delinsGA MANE Select NP_065386.1:n.463-1075_463-1074delinsGA
XR_002957418.1:n.281-14708_281-14707delinsTC