Canonical Allele Identifier: CA337804212
Gene: ISG15 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.949542C>A (hg19) chr1:g.1014162C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.1014162C>A , CM000663.2:g.1014162C>A GRCh38
NC_000001.10:g.949542C>A , CM000663.1:g.949542C>A GRCh37
NC_000001.9:g.939405C>A NCBI36
NG_033033.1:g.5696C>A
NG_033033.2:g.18025C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000624697.4:c.158C>A ENSP00000485643.1:p.Ala53Asp
ENST00000649529.1:c.182C>A MANE Select ENSP00000496832.1:p.Ala61Asp
ENST00000379389.4:c.182C>A ENSP00000368699.4:p.Ala61Asp
ENST00000624652.1:c.158C>A ENSP00000485313.1:p.Ala53Asp
ENST00000624697.3:c.158C>A ENSP00000485643.1:p.Ala53Asp
NM_005101.3:c.182C>A NP_005092.1:p.Ala61Asp
NM_005101.4:c.182C>A MANE Select NP_005092.1:p.Ala61Asp
Search 100 bp 5'
Search 100 bp 3'