Canonical Allele Identifier: CA415756950
Gene: ISG15 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.949612C>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.1014232C>A , CM000663.2:g.1014232C>A GRCh38
NC_000001.10:g.949612C>A , CM000663.1:g.949612C>A GRCh37
NC_000001.9:g.939475C>A NCBI36
NG_033033.1:g.5766C>A
NG_033033.2:g.18095C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000624697.4:c.228C>A ENSP00000485643.1:p.Ile76=
ENST00000649529.1:c.252C>A MANE Select ENSP00000496832.1:p.Ile84=
ENST00000379389.4:c.252C>A ENSP00000368699.4:p.Ile84=
ENST00000624652.1:c.228C>A ENSP00000485313.1:p.Ile76=
ENST00000624697.3:c.228C>A ENSP00000485643.1:p.Ile76=
NM_005101.3:c.252C>A NP_005092.1:p.Ile84=
NM_005101.4:c.252C>A MANE Select NP_005092.1:p.Ile84=
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