Canonical Allele Identifier: CA2742133437
Gene: ISG15 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.1013854_1013855insACGGA , CM000663.2:g.1013854_1013855insACGGA GRCh38
NC_000001.10:g.949234_949235insACGGA , CM000663.1:g.949234_949235insACGGA GRCh37
NC_000001.9:g.939097_939098insACGGA NCBI36
NG_033033.1:g.5388_5389insACGGA
NG_033033.2:g.17717_17718insACGGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000624697.4:c.-21-130_-21-129insACGGA ENSP00000485643.1:n.-21-130_-21-129insACGGA
ENST00000649529.1:c.4-130_4-129insACGGA MANE Select ENSP00000496832.1:n.4-130_4-129insACGGA
ENST00000379389.4:c.4-130_4-129insACGGA ENSP00000368699.4:n.4-130_4-129insACGGA
ENST00000624652.1:c.-21-130_-21-129insACGGA ENSP00000485313.1:n.-21-130_-21-129insACGGA
ENST00000624697.3:c.-21-130_-21-129insACGGA ENSP00000485643.1:n.-21-130_-21-129insACGGA
NM_005101.3:c.4-130_4-129insACGGA NP_005092.1:n.4-130_4-129insACGGA
NM_005101.4:c.4-130_4-129insACGGA MANE Select NP_005092.1:n.4-130_4-129insACGGA