Canonical Allele Identifier: CA1142091738
Gene: ISG15 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.1014138C= , CM000663.2:g.1014138C= GRCh38
NC_000001.10:g.949518C= , CM000663.1:g.949518C= GRCh37
NC_000001.9:g.939381C= NCBI36
NG_033033.1:g.5672C=
NG_033033.2:g.18001C=

Transcript Alleles

HGVS Amino-acid change
ENST00000624697.4:c.134C= ENSP00000485643.1:p.Ala45=
ENST00000649529.1:c.158C= MANE Select ENSP00000496832.1:p.Ala53=
ENST00000379389.4:c.158C= ENSP00000368699.4:p.Ala53=
ENST00000624652.1:c.134C= ENSP00000485313.1:p.Ala45=
ENST00000624697.3:c.134C= ENSP00000485643.1:p.Ala45=
NM_005101.3:c.158C= NP_005092.1:p.Ala53=
NM_005101.4:c.158C= MANE Select NP_005092.1:p.Ala53=