Canonical Allele Identifier: CA2642487191
Gene: ISG15 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.1013862_1013863dup , CM000663.2:g.1013862_1013863dup GRCh38
NC_000001.10:g.949242_949243dup , CM000663.1:g.949242_949243dup GRCh37
NC_000001.9:g.939105_939106dup NCBI36
NG_033033.1:g.5396_5397dup
NG_033033.2:g.17725_17726dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000624697.4:c.-21-122_-21-121dup ENSP00000485643.1:n.-21-122_-21-121dup
ENST00000649529.1:c.4-122_4-121dup MANE Select ENSP00000496832.1:n.4-122_4-121dup
ENST00000379389.4:c.4-122_4-121dup ENSP00000368699.4:n.4-122_4-121dup
ENST00000624652.1:c.-21-122_-21-121dup ENSP00000485313.1:n.-21-122_-21-121dup
ENST00000624697.3:c.-21-122_-21-121dup ENSP00000485643.1:n.-21-122_-21-121dup
NM_005101.3:c.4-122_4-121dup NP_005092.1:n.4-122_4-121dup
NM_005101.4:c.4-122_4-121dup MANE Select NP_005092.1:n.4-122_4-121dup