Canonical Allele Identifier: CA2215668043
Gene: IL27 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.28506292_28506294delinsCCT , CM000678.2:g.28506292_28506294delinsCCT GRCh38
NC_000016.9:g.28517613_28517615delinsCCT , CM000678.1:g.28517613_28517615delinsCCT GRCh37
NC_000016.8:g.28425114_28425116delinsCCT NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000356897.1:c.31+487_31+489delinsAGG MANE Select ENSP00000349365.1:n.31+487_31+489delinsAGG
ENST00000568075.1:c.-362-2244_-362-2242delinsAGG ENSP00000455990.1:n.-362-2244_-362-2242delinsAGG
NM_145659.3:c.31+487_31+489delinsAGG MANE Select NP_663634.2:n.31+487_31+489delinsAGG
XM_011545780.1:c.38-2244_38-2242delinsAGG XP_011544082.1:n.38-2244_38-2242delinsAGG
XM_011545780.2:c.38-2244_38-2242delinsAGG XP_011544082.1:n.38-2244_38-2242delinsAGG
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