Canonical Allele Identifier: CA2642487195
Gene: ISG15 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.1013861_1013862insTGT , CM000663.2:g.1013861_1013862insTGT GRCh38
NC_000001.10:g.949241_949242insTGT , CM000663.1:g.949241_949242insTGT GRCh37
NC_000001.9:g.939104_939105insTGT NCBI36
NG_033033.1:g.5395_5396insTGT
NG_033033.2:g.17724_17725insTGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000624697.4:c.-21-123_-21-122insTGT ENSP00000485643.1:n.-21-123_-21-122insTGT
ENST00000649529.1:c.4-123_4-122insTGT MANE Select ENSP00000496832.1:n.4-123_4-122insTGT
ENST00000379389.4:c.4-123_4-122insTGT ENSP00000368699.4:n.4-123_4-122insTGT
ENST00000624652.1:c.-21-123_-21-122insTGT ENSP00000485313.1:n.-21-123_-21-122insTGT
ENST00000624697.3:c.-21-123_-21-122insTGT ENSP00000485643.1:n.-21-123_-21-122insTGT
NM_005101.3:c.4-123_4-122insTGT NP_005092.1:n.4-123_4-122insTGT
NM_005101.4:c.4-123_4-122insTGT MANE Select NP_005092.1:n.4-123_4-122insTGT