Canonical Allele Identifier: CA1148735153

Gene: ISG15

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1014293G= , CM000663.2:g.1014293G=	GRCh38
NC_000001.10:g.949673G= , CM000663.1:g.949673G=	GRCh37
NC_000001.9:g.939536G=	NCBI36
NG_033033.1:g.5827G=
NG_033033.2:g.18156G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000624697.4:c.289G=	ENSP00000485643.1:p.Ala97=
ENST00000649529.1:c.313G= MANE Select	ENSP00000496832.1:p.Ala105=
ENST00000379389.4:c.313G=	ENSP00000368699.4:p.Ala105=
ENST00000624652.1:c.289G=	ENSP00000485313.1:p.Ala97=
ENST00000624697.3:c.289G=	ENSP00000485643.1:p.Ala97=
NM_005101.3:c.313G=	NP_005092.1:p.Ala105=
NM_005101.4:c.313G= MANE Select	NP_005092.1:p.Ala105=