Canonical Allele Identifier: CA2642487113
Gene: ISG15 HGNC NCBI

Linked Data

gnomAD v4: 1-1013841-T-A
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.1013841T>A , CM000663.2:g.1013841T>A GRCh38
NC_000001.10:g.949221T>A , CM000663.1:g.949221T>A GRCh37
NC_000001.9:g.939084T>A NCBI36
NG_033033.1:g.5375T>A
NG_033033.2:g.17704T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000624697.4:c.-21-143T>A ENSP00000485643.1:n.-21-143T>A
ENST00000649529.1:c.4-143T>A MANE Select ENSP00000496832.1:n.4-143T>A
ENST00000379389.4:c.4-143T>A ENSP00000368699.4:n.4-143T>A
ENST00000624652.1:c.-21-143T>A ENSP00000485313.1:n.-21-143T>A
ENST00000624697.3:c.-21-143T>A ENSP00000485643.1:n.-21-143T>A
NM_005101.3:c.4-143T>A NP_005092.1:n.4-143T>A
NM_005101.4:c.4-143T>A MANE Select NP_005092.1:n.4-143T>A
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