Canonical Allele Identifier: CA16725028

Gene: ISG15

Linked Data

• dbSNP Id: rs1126573
• MyVariant Identifiers: chr1:g.949370G>A (hg19) ; chr1:g.1013990G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1013990G>A , CM000663.2:g.1013990G>A	GRCh38
NC_000001.10:g.949370G>A , CM000663.1:g.949370G>A	GRCh37
NC_000001.9:g.939233G>A	NCBI36
NG_033033.1:g.5524G>A
NG_033033.2:g.17853G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000624697.4:c.-15G>A	ENSP00000485643.1:n.-15G>A
ENST00000649529.1:c.10G>A MANE Select	ENSP00000496832.1:p.Asp4Asn
ENST00000379389.4:c.10G>A	ENSP00000368699.4:p.Asp4Asn
ENST00000624652.1:c.-15G>A	ENSP00000485313.1:n.-15G>A
ENST00000624697.3:c.-15G>A	ENSP00000485643.1:n.-15G>A
NM_005101.3:c.10G>A	NP_005092.1:p.Asp4Asn
NM_005101.4:c.10G>A MANE Select	NP_005092.1:p.Asp4Asn