Canonical Allele Identifier: CA337804817

Gene: ISG15

Linked Data

• MyVariant Identifiers: chr1:g.949642C>A (hg19) ; chr1:g.1014262C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1014262C>A , CM000663.2:g.1014262C>A	GRCh38
NC_000001.10:g.949642C>A , CM000663.1:g.949642C>A	GRCh37
NC_000001.9:g.939505C>A	NCBI36
NG_033033.1:g.5796C>A
NG_033033.2:g.18125C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000624697.4:c.258C>A	ENSP00000485643.1:p.Ser86Arg
ENST00000649529.1:c.282C>A MANE Select	ENSP00000496832.1:p.Ser94Arg
ENST00000379389.4:c.282C>A	ENSP00000368699.4:p.Ser94Arg
ENST00000624652.1:c.258C>A	ENSP00000485313.1:p.Ser86Arg
ENST00000624697.3:c.258C>A	ENSP00000485643.1:p.Ser86Arg
NM_005101.3:c.282C>A	NP_005092.1:p.Ser94Arg
NM_005101.4:c.282C>A MANE Select	NP_005092.1:p.Ser94Arg