Canonical Allele Identifier: CA2742133451
Gene: ISG15 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.1013866_1013867insTAT , CM000663.2:g.1013866_1013867insTAT GRCh38
NC_000001.10:g.949246_949247insTAT , CM000663.1:g.949246_949247insTAT GRCh37
NC_000001.9:g.939109_939110insTAT NCBI36
NG_033033.1:g.5400_5401insTAT
NG_033033.2:g.17729_17730insTAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000624697.4:c.-21-118_-21-117insTAT ENSP00000485643.1:n.-21-118_-21-117insTAT
ENST00000649529.1:c.4-118_4-117insTAT MANE Select ENSP00000496832.1:n.4-118_4-117insTAT
ENST00000379389.4:c.4-118_4-117insTAT ENSP00000368699.4:n.4-118_4-117insTAT
ENST00000624652.1:c.-21-118_-21-117insTAT ENSP00000485313.1:n.-21-118_-21-117insTAT
ENST00000624697.3:c.-21-118_-21-117insTAT ENSP00000485643.1:n.-21-118_-21-117insTAT
NM_005101.3:c.4-118_4-117insTAT NP_005092.1:n.4-118_4-117insTAT
NM_005101.4:c.4-118_4-117insTAT MANE Select NP_005092.1:n.4-118_4-117insTAT