Canonical Allele Identifier: CA337803955
Gene: ISG15 HGNC NCBI

Linked Data

gnomAD v4: 1-1014124-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.1014124C>A , CM000663.2:g.1014124C>A GRCh38
NC_000001.10:g.949504C>A , CM000663.1:g.949504C>A GRCh37
NC_000001.9:g.939367C>A NCBI36
NG_033033.1:g.5658C>A
NG_033033.2:g.17987C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000624697.4:c.120C>A ENSP00000485643.1:p.His40Gln
ENST00000649529.1:c.144C>A MANE Select ENSP00000496832.1:p.His48Gln
ENST00000379389.4:c.144C>A ENSP00000368699.4:p.His48Gln
ENST00000624652.1:c.120C>A ENSP00000485313.1:p.His40Gln
ENST00000624697.3:c.120C>A ENSP00000485643.1:p.His40Gln
NM_005101.3:c.144C>A NP_005092.1:p.His48Gln
NM_005101.4:c.144C>A MANE Select NP_005092.1:p.His48Gln