Canonical Allele Identifier: CA2642487323
Gene: ISG15 HGNC NCBI

Linked Data

gnomAD v4: 1-1013887-T-TG

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.1013888dup , CM000663.2:g.1013888dup GRCh38
NC_000001.10:g.949268dup , CM000663.1:g.949268dup GRCh37
NC_000001.9:g.939131dup NCBI36
NG_033033.1:g.5422dup
NG_033033.2:g.17751dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000624697.4:c.-21-96dup ENSP00000485643.1:n.-21-96dup
ENST00000649529.1:c.4-96dup MANE Select ENSP00000496832.1:n.4-96dup
ENST00000379389.4:c.4-96dup ENSP00000368699.4:n.4-96dup
ENST00000624652.1:c.-21-96dup ENSP00000485313.1:n.-21-96dup
ENST00000624697.3:c.-21-96dup ENSP00000485643.1:n.-21-96dup
NM_005101.3:c.4-96dup NP_005092.1:n.4-96dup
NM_005101.4:c.4-96dup MANE Select NP_005092.1:n.4-96dup