Canonical Allele Identifier: CA16725727
Gene: ISG15 HGNC NCBI

Linked Data

dbSNP Id: rs867281625

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.1014339A>C , CM000663.2:g.1014339A>C GRCh38
NC_000001.10:g.949719A>C , CM000663.1:g.949719A>C GRCh37
NC_000001.9:g.939582A>C NCBI36
NG_033033.1:g.5873A>C
NG_033033.2:g.18202A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000624697.4:c.335A>C ENSP00000485643.1:p.Asp112Ala
ENST00000649529.1:c.359A>C MANE Select ENSP00000496832.1:p.Asp120Ala
ENST00000379389.4:c.359A>C ENSP00000368699.4:p.Asp120Ala
ENST00000624652.1:c.335A>C ENSP00000485313.1:p.Asp112Ala
ENST00000624697.3:c.335A>C ENSP00000485643.1:p.Asp112Ala
NM_005101.3:c.359A>C NP_005092.1:p.Asp120Ala
NM_005101.4:c.359A>C MANE Select NP_005092.1:p.Asp120Ala