Canonical Allele Identifier: CA2642487192
Gene: ISG15 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.1013861_1013862insTAAGT , CM000663.2:g.1013861_1013862insTAAGT GRCh38
NC_000001.10:g.949241_949242insTAAGT , CM000663.1:g.949241_949242insTAAGT GRCh37
NC_000001.9:g.939104_939105insTAAGT NCBI36
NG_033033.1:g.5395_5396insTAAGT
NG_033033.2:g.17724_17725insTAAGT

Transcript Alleles

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