Canonical Allele Identifier: CA337803981
Gene: ISG15 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.949508A>T (hg19) chr1:g.1014128A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.1014128A>T , CM000663.2:g.1014128A>T GRCh38
NC_000001.10:g.949508A>T , CM000663.1:g.949508A>T GRCh37
NC_000001.9:g.939371A>T NCBI36
NG_033033.1:g.5662A>T
NG_033033.2:g.17991A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000624697.4:c.124A>T ENSP00000485643.1:p.Ser42Cys
ENST00000649529.1:c.148A>T MANE Select ENSP00000496832.1:p.Ser50Cys
ENST00000379389.4:c.148A>T ENSP00000368699.4:p.Ser50Cys
ENST00000624652.1:c.124A>T ENSP00000485313.1:p.Ser42Cys
ENST00000624697.3:c.124A>T ENSP00000485643.1:p.Ser42Cys
NM_005101.3:c.148A>T NP_005092.1:p.Ser50Cys
NM_005101.4:c.148A>T MANE Select NP_005092.1:p.Ser50Cys
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