Canonical Allele Identifier: CA1148733770

Gene: ISG15

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1014053G= , CM000663.2:g.1014053G=	GRCh38
NC_000001.10:g.949433G= , CM000663.1:g.949433G=	GRCh37
NC_000001.9:g.939296G=	NCBI36
NG_033033.1:g.5587G=
NG_033033.2:g.17916G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000624697.4:c.49G=	ENSP00000485643.1:p.Val17=
ENST00000649529.1:c.73G= MANE Select	ENSP00000496832.1:p.Val25=
ENST00000379389.4:c.73G=	ENSP00000368699.4:p.Val25=
ENST00000624652.1:c.49G=	ENSP00000485313.1:p.Val17=
ENST00000624697.3:c.49G=	ENSP00000485643.1:p.Val17=
NM_005101.3:c.73G=	NP_005092.1:p.Val25=
NM_005101.4:c.73G= MANE Select	NP_005092.1:p.Val25=