Canonical Allele Identifier: CA1148734784
Gene: ISG15 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.1014234_1014235delinsTG , CM000663.2:g.1014234_1014235delinsTG GRCh38
NC_000001.10:g.949614_949615delinsTG , CM000663.1:g.949614_949615delinsTG GRCh37
NC_000001.9:g.939477_939478delinsTG NCBI36
NG_033033.1:g.5768_5769delinsTG
NG_033033.2:g.18097_18098delinsTG

Transcript Alleles

HGVS Amino-acid change
ENST00000624697.4:c.230_231delinsTG ENSP00000485643.1:p.Leu77=
ENST00000649529.1:c.254_255delinsTG MANE Select ENSP00000496832.1:p.Leu85=
ENST00000379389.4:c.254_255delinsTG ENSP00000368699.4:p.Leu85=
ENST00000624652.1:c.230_231delinsTG ENSP00000485313.1:p.Leu77=
ENST00000624697.3:c.230_231delinsTG ENSP00000485643.1:p.Leu77=
NM_005101.3:c.254_255delinsTG NP_005092.1:p.Leu85=
NM_005101.4:c.254_255delinsTG MANE Select NP_005092.1:p.Leu85=
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