Canonical Allele Identifier: CA1143542619

Gene: ISG15

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1014020G= , CM000663.2:g.1014020G=	GRCh38
NC_000001.10:g.949400G= , CM000663.1:g.949400G=	GRCh37
NC_000001.9:g.939263G=	NCBI36
NG_033033.1:g.5554G=
NG_033033.2:g.17883G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000624697.4:c.16G=	ENSP00000485643.1:p.Glu6=
ENST00000649529.1:c.40G= MANE Select	ENSP00000496832.1:p.Glu14=
ENST00000379389.4:c.40G=	ENSP00000368699.4:p.Glu14=
ENST00000624652.1:c.16G=	ENSP00000485313.1:p.Glu6=
ENST00000624697.3:c.16G=	ENSP00000485643.1:p.Glu6=
NM_005101.3:c.40G=	NP_005092.1:p.Glu14=
NM_005101.4:c.40G= MANE Select	NP_005092.1:p.Glu14=