Canonical Allele Identifier: CA1490361289

Gene: IL21

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.122613968_122613969delinsAG , CM000666.2:g.122613968_122613969delinsAG	GRCh38
NC_000004.11:g.123535123_123535124delinsAG , CM000666.1:g.123535123_123535124delinsAG	GRCh37
NC_000004.10:g.123754573_123754574delinsAG	NCBI36
NG_031966.1:g.12089_12090delinsCT
NG_031966.2:g.12098_12099delinsCT

Transcript Alleles

HGVS	Amino-acid change
ENST00000611104.2:c.361-1041_361-1040delinsCT	ENSP00000477555.1:n.361-1041_361-1040delinsCT
ENST00000647784.1:n.213-1041_213-1040delinsCT
ENST00000648588.1:c.361-1041_361-1040delinsCT MANE Select	ENSP00000497915.1:n.361-1041_361-1040delinsCT
ENST00000264497.7:c.361-1041_361-1040delinsCT	ENSP00000264497.3:n.361-1041_361-1040delinsCT
ENST00000611104.1:c.361-1041_361-1040delinsCT	ENSP00000477555.1:n.361-1041_361-1040delinsCT
NM_001207006.2:c.361-1041_361-1040delinsCT	NP_001193935.1:n.361-1041_361-1040delinsCT
NM_021803.3:c.361-1041_361-1040delinsCT	NP_068575.1:n.361-1041_361-1040delinsCT
NM_021803.4:c.361-1041_361-1040delinsCT MANE Select	NP_068575.1:n.361-1041_361-1040delinsCT
NM_001207006.3:c.361-1041_361-1040delinsCT	NP_001193935.1:n.361-1041_361-1040delinsCT