Canonical Allele Identifier: CA337803978
Gene: ISG15 HGNC NCBI

Linked Data

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

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

Transcript Alleles

HGVS Amino-acid change
ENST00000624697.4:c.124A>G ENSP00000485643.1:p.Ser42Gly
ENST00000649529.1:c.148A>G MANE Select ENSP00000496832.1:p.Ser50Gly
ENST00000379389.4:c.148A>G ENSP00000368699.4:p.Ser50Gly
ENST00000624652.1:c.124A>G ENSP00000485313.1:p.Ser42Gly
ENST00000624697.3:c.124A>G ENSP00000485643.1:p.Ser42Gly
NM_005101.3:c.148A>G NP_005092.1:p.Ser50Gly
NM_005101.4:c.148A>G MANE Select NP_005092.1:p.Ser50Gly
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