Canonical Allele Identifier: CA2642487320
Gene: ISG15 HGNC NCBI

Linked Data

gnomAD v4: 1-1013886-CT-C

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.1013887del , CM000663.2:g.1013887del GRCh38
NC_000001.10:g.949267del , CM000663.1:g.949267del GRCh37
NC_000001.9:g.939130del NCBI36
NG_033033.1:g.5421del
NG_033033.2:g.17750del

Transcript Alleles

HGVS Amino-acid Change
ENST00000624697.4:c.-21-97del ENSP00000485643.1:n.-21-97del
ENST00000649529.1:c.4-97del MANE Select ENSP00000496832.1:n.4-97del
ENST00000379389.4:c.4-97del ENSP00000368699.4:n.4-97del
ENST00000624652.1:c.-21-97del ENSP00000485313.1:n.-21-97del
ENST00000624697.3:c.-21-97del ENSP00000485643.1:n.-21-97del
NM_005101.3:c.4-97del NP_005092.1:n.4-97del
NM_005101.4:c.4-97del MANE Select NP_005092.1:n.4-97del