Canonical Allele Identifier: CA337803542
Gene: ISG15 HGNC NCBI

Linked Data

dbSNP Id: rs1459040516

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.1014032T>C , CM000663.2:g.1014032T>C GRCh38
NC_000001.10:g.949412T>C , CM000663.1:g.949412T>C GRCh37
NC_000001.9:g.939275T>C NCBI36
NG_033033.1:g.5566T>C
NG_033033.2:g.17895T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000624697.4:c.28T>C ENSP00000485643.1:p.Ser10Pro
ENST00000649529.1:c.52T>C MANE Select ENSP00000496832.1:p.Ser18Pro
ENST00000379389.4:c.52T>C ENSP00000368699.4:p.Ser18Pro
ENST00000624652.1:c.28T>C ENSP00000485313.1:p.Ser10Pro
ENST00000624697.3:c.28T>C ENSP00000485643.1:p.Ser10Pro
NM_005101.3:c.52T>C NP_005092.1:p.Ser18Pro
NM_005101.4:c.52T>C MANE Select NP_005092.1:p.Ser18Pro