Canonical Allele Identifier: CA1143930946
Gene: ISG15 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.1014130C= , CM000663.2:g.1014130C= GRCh38
NC_000001.10:g.949510C= , CM000663.1:g.949510C= GRCh37
NC_000001.9:g.939373C= NCBI36
NG_033033.1:g.5664C=
NG_033033.2:g.17993C=

Transcript Alleles

HGVS Amino-acid change
ENST00000624697.4:c.126C= ENSP00000485643.1:p.Ser42=
ENST00000649529.1:c.150C= MANE Select ENSP00000496832.1:p.Ser50=
ENST00000379389.4:c.150C= ENSP00000368699.4:p.Ser50=
ENST00000624652.1:c.126C= ENSP00000485313.1:p.Ser42=
ENST00000624697.3:c.126C= ENSP00000485643.1:p.Ser42=
NM_005101.3:c.150C= NP_005092.1:p.Ser50=
NM_005101.4:c.150C= MANE Select NP_005092.1:p.Ser50=