Canonical Allele Identifier: CA1490361295
Gene: IL21 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.122613985_122613986delinsCT , CM000666.2:g.122613985_122613986delinsCT GRCh38
NC_000004.11:g.123535140_123535141delinsCT , CM000666.1:g.123535140_123535141delinsCT GRCh37
NC_000004.10:g.123754590_123754591delinsCT NCBI36
NG_031966.1:g.12072_12073delinsAG
NG_031966.2:g.12081_12082delinsAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000611104.2:c.361-1058_361-1057delinsAG ENSP00000477555.1:n.361-1058_361-1057delinsAG
ENST00000647784.1:n.213-1058_213-1057delinsAG
ENST00000648588.1:c.361-1058_361-1057delinsAG MANE Select ENSP00000497915.1:n.361-1058_361-1057delinsAG
ENST00000264497.7:c.361-1058_361-1057delinsAG ENSP00000264497.3:n.361-1058_361-1057delinsAG
ENST00000611104.1:c.361-1058_361-1057delinsAG ENSP00000477555.1:n.361-1058_361-1057delinsAG
NM_001207006.2:c.361-1058_361-1057delinsAG NP_001193935.1:n.361-1058_361-1057delinsAG
NM_021803.3:c.361-1058_361-1057delinsAG NP_068575.1:n.361-1058_361-1057delinsAG
NM_021803.4:c.361-1058_361-1057delinsAG MANE Select NP_068575.1:n.361-1058_361-1057delinsAG
NM_001207006.3:c.361-1058_361-1057delinsAG NP_001193935.1:n.361-1058_361-1057delinsAG