Canonical Allele Identifier: CA1148224140
Gene: ISG15 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.1014317_1014319delinsGGG , CM000663.2:g.1014317_1014319delinsGGG GRCh38
NC_000001.10:g.949697_949699delinsGGG , CM000663.1:g.949697_949699delinsGGG GRCh37
NC_000001.9:g.939560_939562delinsGGG NCBI36
NG_033033.1:g.5851_5853delinsGGG
NG_033033.2:g.18180_18182delinsGGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000624697.4:c.313_315delinsGGG ENSP00000485643.1:p.Gly105=
ENST00000649529.1:c.337_339delinsGGG MANE Select ENSP00000496832.1:p.Gly113=
ENST00000379389.4:c.337_339delinsGGG ENSP00000368699.4:p.Gly113=
ENST00000624652.1:c.313_315delinsGGG ENSP00000485313.1:p.Gly105=
ENST00000624697.3:c.313_315delinsGGG ENSP00000485643.1:p.Gly105=
NM_005101.3:c.337_339delinsGGG NP_005092.1:p.Gly113=
NM_005101.4:c.337_339delinsGGG MANE Select NP_005092.1:p.Gly113=