Canonical Allele Identifier: CA2742133450
Gene: ISG15 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.1013867_1013868del , CM000663.2:g.1013867_1013868del GRCh38
NC_000001.10:g.949247_949248del , CM000663.1:g.949247_949248del GRCh37
NC_000001.9:g.939110_939111del NCBI36
NG_033033.1:g.5401_5402del
NG_033033.2:g.17730_17731del

Transcript Alleles

HGVS Amino-acid Change
ENST00000624697.4:c.-21-117_-21-116del ENSP00000485643.1:n.-21-117_-21-116del
ENST00000649529.1:c.4-117_4-116del MANE Select ENSP00000496832.1:n.4-117_4-116del
ENST00000379389.4:c.4-117_4-116del ENSP00000368699.4:n.4-117_4-116del
ENST00000624652.1:c.-21-117_-21-116del ENSP00000485313.1:n.-21-117_-21-116del
ENST00000624697.3:c.-21-117_-21-116del ENSP00000485643.1:n.-21-117_-21-116del
NM_005101.3:c.4-117_4-116del NP_005092.1:n.4-117_4-116del
NM_005101.4:c.4-117_4-116del MANE Select NP_005092.1:n.4-117_4-116del