Canonical Allele Identifier: CA2742133439
Gene: ISG15 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.1013859_1013865del , CM000663.2:g.1013859_1013865del GRCh38
NC_000001.10:g.949239_949245del , CM000663.1:g.949239_949245del GRCh37
NC_000001.9:g.939102_939108del NCBI36
NG_033033.1:g.5393_5399del
NG_033033.2:g.17722_17728del

Transcript Alleles

HGVS Amino-acid Change
ENST00000624697.4:c.-21-125_-21-119del ENSP00000485643.1:n.-21-125_-21-119del
ENST00000649529.1:c.4-125_4-119del MANE Select ENSP00000496832.1:n.4-125_4-119del
ENST00000379389.4:c.4-125_4-119del ENSP00000368699.4:n.4-125_4-119del
ENST00000624652.1:c.-21-125_-21-119del ENSP00000485313.1:n.-21-125_-21-119del
ENST00000624697.3:c.-21-125_-21-119del ENSP00000485643.1:n.-21-125_-21-119del
NM_005101.3:c.4-125_4-119del NP_005092.1:n.4-125_4-119del
NM_005101.4:c.4-125_4-119del MANE Select NP_005092.1:n.4-125_4-119del