Canonical Allele Identifier: CA2574198261
Gene: ISG15 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.1013928T>C , CM000663.2:g.1013928T>C GRCh38
NC_000001.10:g.949308T>C , CM000663.1:g.949308T>C GRCh37
NC_000001.9:g.939171T>C NCBI36
NG_033033.1:g.5462T>C
NG_033033.2:g.17791T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000624697.4:c.-21-56T>C ENSP00000485643.1:n.-21-56T>C
ENST00000649529.1:c.4-56T>C MANE Select ENSP00000496832.1:n.4-56T>C
ENST00000379389.4:c.4-56T>C ENSP00000368699.4:n.4-56T>C
ENST00000624652.1:c.-21-56T>C ENSP00000485313.1:n.-21-56T>C
ENST00000624697.3:c.-21-56T>C ENSP00000485643.1:n.-21-56T>C
NM_005101.3:c.4-56T>C NP_005092.1:n.4-56T>C
NM_005101.4:c.4-56T>C MANE Select NP_005092.1:n.4-56T>C
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