Canonical Allele Identifier: CA1146146792
Gene: ISG15 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.1013826A= , CM000663.2:g.1013826A= GRCh38
NC_000001.10:g.949206A= , CM000663.1:g.949206A= GRCh37
NC_000001.9:g.939069A= NCBI36
NG_033033.1:g.5360A=
NG_033033.2:g.17689A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000624697.4:c.-21-158A= ENSP00000485643.1:n.-21-158A=
ENST00000649529.1:c.4-158A= MANE Select ENSP00000496832.1:n.4-158A=
ENST00000379389.4:c.4-158A= ENSP00000368699.4:n.4-158A=
ENST00000624652.1:c.-21-158A= ENSP00000485313.1:n.-21-158A=
ENST00000624697.3:c.-21-158A= ENSP00000485643.1:n.-21-158A=
NM_005101.3:c.4-158A= NP_005092.1:n.4-158A=
NM_005101.4:c.4-158A= MANE Select NP_005092.1:n.4-158A=