Canonical Allele Identifier: CA1490361218
Gene: IL21 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.122613803_122613804delinsAG , CM000666.2:g.122613803_122613804delinsAG GRCh38
NC_000004.11:g.123534958_123534959delinsAG , CM000666.1:g.123534958_123534959delinsAG GRCh37
NC_000004.10:g.123754408_123754409delinsAG NCBI36
NG_031966.1:g.12254_12255delinsCT
NG_031966.2:g.12263_12264delinsCT

Transcript Alleles

HGVS Amino-acid change
ENST00000611104.2:c.361-876_361-875delinsCT ENSP00000477555.1:n.361-876_361-875delins...
ENST00000647784.1:n.213-876_213-875delinsCT
ENST00000648588.1:c.361-876_361-875delinsCT MANE Select ENSP00000497915.1:n.361-876_361-875delins...
ENST00000264497.7:c.361-876_361-875delinsCT ENSP00000264497.3:n.361-876_361-875delins...
ENST00000611104.1:c.361-876_361-875delinsCT ENSP00000477555.1:n.361-876_361-875delins...
NM_001207006.2:c.361-876_361-875delinsCT NP_001193935.1:n.361-876_361-875delinsCT
NM_021803.3:c.361-876_361-875delinsCT NP_068575.1:n.361-876_361-875delinsCT
NM_021803.4:c.361-876_361-875delinsCT MANE Select NP_068575.1:n.361-876_361-875delinsCT
NM_001207006.3:c.361-876_361-875delinsCT NP_001193935.1:n.361-876_361-875delinsCT
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