Canonical Allele Identifier: CA1148845538
Gene: ISG15 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.1013858G= , CM000663.2:g.1013858G= GRCh38
NC_000001.10:g.949238G= , CM000663.1:g.949238G= GRCh37
NC_000001.9:g.939101G= NCBI36
NG_033033.1:g.5392G=
NG_033033.2:g.17721G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000624697.4:c.-21-126G= ENSP00000485643.1:n.-21-126G=
ENST00000649529.1:c.4-126G= MANE Select ENSP00000496832.1:n.4-126G=
ENST00000379389.4:c.4-126G= ENSP00000368699.4:n.4-126G=
ENST00000624652.1:c.-21-126G= ENSP00000485313.1:n.-21-126G=
ENST00000624697.3:c.-21-126G= ENSP00000485643.1:n.-21-126G=
NM_005101.3:c.4-126G= NP_005092.1:n.4-126G=
NM_005101.4:c.4-126G= MANE Select NP_005092.1:n.4-126G=