Canonical Allele Identifier: CA2642487276
Gene: ISG15 HGNC NCBI

Linked Data

gnomAD v4: 1-1013873-A-AT
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.1013873_1013874insT , CM000663.2:g.1013873_1013874insT GRCh38
NC_000001.10:g.949253_949254insT , CM000663.1:g.949253_949254insT GRCh37
NC_000001.9:g.939116_939117insT NCBI36
NG_033033.1:g.5407_5408insT
NG_033033.2:g.17736_17737insT

Transcript Alleles

HGVS Amino-acid Change
ENST00000624697.4:c.-21-111_-21-110insT ENSP00000485643.1:n.-21-111_-21-110insT
ENST00000649529.1:c.4-111_4-110insT MANE Select ENSP00000496832.1:n.4-111_4-110insT
ENST00000379389.4:c.4-111_4-110insT ENSP00000368699.4:n.4-111_4-110insT
ENST00000624652.1:c.-21-111_-21-110insT ENSP00000485313.1:n.-21-111_-21-110insT
ENST00000624697.3:c.-21-111_-21-110insT ENSP00000485643.1:n.-21-111_-21-110insT
NM_005101.3:c.4-111_4-110insT NP_005092.1:n.4-111_4-110insT
NM_005101.4:c.4-111_4-110insT MANE Select NP_005092.1:n.4-111_4-110insT
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