Canonical Allele Identifier: CA2591187466
Gene: ISG15 HGNC NCBI

Linked Data

dbSNP Id: rs2100541641
gnomAD v3: 1-1013833-TC-T
gnomAD v4: 1-1013833-TC-T

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.1013834del , CM000663.2:g.1013834del GRCh38
NC_000001.10:g.949214del , CM000663.1:g.949214del GRCh37
NC_000001.9:g.939077del NCBI36
NG_033033.1:g.5368del
NG_033033.2:g.17697del

Transcript Alleles

HGVS Amino-acid Change
ENST00000624697.4:c.-21-150del ENSP00000485643.1:n.-21-150del
ENST00000649529.1:c.4-150del MANE Select ENSP00000496832.1:n.4-150del
ENST00000379389.4:c.4-150del ENSP00000368699.4:n.4-150del
ENST00000624652.1:c.-21-150del ENSP00000485313.1:n.-21-150del
ENST00000624697.3:c.-21-150del ENSP00000485643.1:n.-21-150del
NM_005101.3:c.4-150del NP_005092.1:n.4-150del
NM_005101.4:c.4-150del MANE Select NP_005092.1:n.4-150del