Canonical Allele Identifier: CA337804807

Gene: ISG15

Linked Data

• gnomAD v4: 1-1014260-A-C
• MyVariant Identifiers: chr1:g.949640A>C (hg19) ; chr1:g.1014260A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1014260A>C , CM000663.2:g.1014260A>C	GRCh38
NC_000001.10:g.949640A>C , CM000663.1:g.949640A>C	GRCh37
NC_000001.9:g.939503A>C	NCBI36
NG_033033.1:g.5794A>C
NG_033033.2:g.18123A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000624697.4:c.256A>C	ENSP00000485643.1:p.Ser86Arg
ENST00000649529.1:c.280A>C MANE Select	ENSP00000496832.1:p.Ser94Arg
ENST00000379389.4:c.280A>C	ENSP00000368699.4:p.Ser94Arg
ENST00000624652.1:c.256A>C	ENSP00000485313.1:p.Ser86Arg
ENST00000624697.3:c.256A>C	ENSP00000485643.1:p.Ser86Arg
NM_005101.3:c.280A>C	NP_005092.1:p.Ser94Arg
NM_005101.4:c.280A>C MANE Select	NP_005092.1:p.Ser94Arg