Canonical Allele Identifier: CA1148734286

Gene: ISG15

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1014135T= , CM000663.2:g.1014135T=	GRCh38
NC_000001.10:g.949515T= , CM000663.1:g.949515T=	GRCh37
NC_000001.9:g.939378T=	NCBI36
NG_033033.1:g.5669T=
NG_033033.2:g.17998T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000624697.4:c.131T=	ENSP00000485643.1:p.Val44=
ENST00000649529.1:c.155T= MANE Select	ENSP00000496832.1:p.Val52=
ENST00000379389.4:c.155T=	ENSP00000368699.4:p.Val52=
ENST00000624652.1:c.131T=	ENSP00000485313.1:p.Val44=
ENST00000624697.3:c.131T=	ENSP00000485643.1:p.Val44=
NM_005101.3:c.155T=	NP_005092.1:p.Val52=
NM_005101.4:c.155T= MANE Select	NP_005092.1:p.Val52=