Canonical Allele Identifier: CA337803516
Gene: ISG15 HGNC NCBI

Linked Data

gnomAD v4: 1-1014026-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.1014026C>A , CM000663.2:g.1014026C>A GRCh38
NC_000001.10:g.949406C>A , CM000663.1:g.949406C>A GRCh37
NC_000001.9:g.939269C>A NCBI36
NG_033033.1:g.5560C>A
NG_033033.2:g.17889C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000624697.4:c.22C>A ENSP00000485643.1:p.Gln8Lys
ENST00000649529.1:c.46C>A MANE Select ENSP00000496832.1:p.Gln16Lys
ENST00000379389.4:c.46C>A ENSP00000368699.4:p.Gln16Lys
ENST00000624652.1:c.22C>A ENSP00000485313.1:p.Gln8Lys
ENST00000624697.3:c.22C>A ENSP00000485643.1:p.Gln8Lys
NM_005101.3:c.46C>A NP_005092.1:p.Gln16Lys
NM_005101.4:c.46C>A MANE Select NP_005092.1:p.Gln16Lys