Canonical Allele Identifier: CA2043864968

Gene: IL22

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.68249934_68249937delinsATTT , CM000674.2:g.68249934_68249937delinsATTT	GRCh38
NC_000012.11:g.68643714_68643717delinsATTT , CM000674.1:g.68643714_68643717delinsATTT	GRCh37
NC_000012.10:g.66929981_66929984delinsATTT	NCBI36
NG_060763.1:g.8668_8671delinsAAAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328087.6:c.463-1061_463-1058delinsAAAT	ENSP00000329384.4:n.463-1061_463-1058delinsAAAT
ENST00000538666.6:c.463-1061_463-1058delinsAAAT MANE Select	ENSP00000442424.1:n.463-1061_463-1058delinsAAAT
ENST00000328087.5:c.463-1061_463-1058delinsAAAT	ENSP00000329384.4:n.463-1061_463-1058delinsAAAT
ENST00000538666.5:c.463-1061_463-1058delinsAAAT	ENSP00000442424.1:n.463-1061_463-1058delinsAAAT
NM_020525.4:c.463-1061_463-1058delinsAAAT	NP_065386.1:n.463-1061_463-1058delinsAAAT
XR_945055.1:n.265-14724_265-14721delinsATTT
NM_020525.5:c.463-1061_463-1058delinsAAAT MANE Select	NP_065386.1:n.463-1061_463-1058delinsAAAT
XR_002957418.1:n.281-14724_281-14721delinsATTT