Canonical Allele Identifier: CA1148734815
Gene: ISG15 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.1014236G= , CM000663.2:g.1014236G= GRCh38
NC_000001.10:g.949616G= , CM000663.1:g.949616G= GRCh37
NC_000001.9:g.939479G= NCBI36
NG_033033.1:g.5770G=
NG_033033.2:g.18099G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000624697.4:c.232G= ENSP00000485643.1:p.Val78=
ENST00000649529.1:c.256G= MANE Select ENSP00000496832.1:p.Val86=
ENST00000379389.4:c.256G= ENSP00000368699.4:p.Val86=
ENST00000624652.1:c.232G= ENSP00000485313.1:p.Val78=
ENST00000624697.3:c.232G= ENSP00000485643.1:p.Val78=
NM_005101.3:c.256G= NP_005092.1:p.Val86=
NM_005101.4:c.256G= MANE Select NP_005092.1:p.Val86=