Canonical Allele Identifier: CA1148845988
Gene: ISG15 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.1013980G= , CM000663.2:g.1013980G= GRCh38
NC_000001.10:g.949360G= , CM000663.1:g.949360G= GRCh37
NC_000001.9:g.939223G= NCBI36
NG_033033.1:g.5514G=
NG_033033.2:g.17843G=

Transcript Alleles

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