Canonical Allele Identifier: CA415345835
Gene: ISG15 HGNC NCBI

Linked Data

gnomAD v4: 1-1014292-G-A
MyVariant Identifiers: chr1:g.949672G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.1014292G>A , CM000663.2:g.1014292G>A GRCh38
NC_000001.10:g.949672G>A , CM000663.1:g.949672G>A GRCh37
NC_000001.9:g.939535G>A NCBI36
NG_033033.1:g.5826G>A
NG_033033.2:g.18155G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000624697.4:c.288G>A ENSP00000485643.1:p.Val96=
ENST00000649529.1:c.312G>A MANE Select ENSP00000496832.1:p.Val104=
ENST00000379389.4:c.312G>A ENSP00000368699.4:p.Val104=
ENST00000624652.1:c.288G>A ENSP00000485313.1:p.Val96=
ENST00000624697.3:c.288G>A ENSP00000485643.1:p.Val96=
NM_005101.3:c.312G>A NP_005092.1:p.Val104=
NM_005101.4:c.312G>A MANE Select NP_005092.1:p.Val104=
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