Canonical Allele Identifier: CA2043864965

Gene: IL22

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.68249932_68249933delinsGA , CM000674.2:g.68249932_68249933delinsGA	GRCh38
NC_000012.11:g.68643712_68643713delinsGA , CM000674.1:g.68643712_68643713delinsGA	GRCh37
NC_000012.10:g.66929979_66929980delinsGA	NCBI36
NG_060763.1:g.8672_8673delinsTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328087.6:c.463-1057_463-1056delinsTC	ENSP00000329384.4:n.463-1057_463-1056delinsTC
ENST00000538666.6:c.463-1057_463-1056delinsTC MANE Select	ENSP00000442424.1:n.463-1057_463-1056delinsTC
ENST00000328087.5:c.463-1057_463-1056delinsTC	ENSP00000329384.4:n.463-1057_463-1056delinsTC
ENST00000538666.5:c.463-1057_463-1056delinsTC	ENSP00000442424.1:n.463-1057_463-1056delinsTC
NM_020525.4:c.463-1057_463-1056delinsTC	NP_065386.1:n.463-1057_463-1056delinsTC
XR_945055.1:n.265-14726_265-14725delinsGA
NM_020525.5:c.463-1057_463-1056delinsTC MANE Select	NP_065386.1:n.463-1057_463-1056delinsTC
XR_002957418.1:n.281-14726_281-14725delinsGA