Canonical Allele Identifier: CA2642487202
Gene: ISG15 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.1013860_1013861insACTAG , CM000663.2:g.1013860_1013861insACTAG GRCh38
NC_000001.10:g.949240_949241insACTAG , CM000663.1:g.949240_949241insACTAG GRCh37
NC_000001.9:g.939103_939104insACTAG NCBI36
NG_033033.1:g.5394_5395insACTAG
NG_033033.2:g.17723_17724insACTAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000624697.4:c.-21-124_-21-123insACTAG ENSP00000485643.1:n.-21-124_-21-123insACTAG
ENST00000649529.1:c.4-124_4-123insACTAG MANE Select ENSP00000496832.1:n.4-124_4-123insACTAG
ENST00000379389.4:c.4-124_4-123insACTAG ENSP00000368699.4:n.4-124_4-123insACTAG
ENST00000624652.1:c.-21-124_-21-123insACTAG ENSP00000485313.1:n.-21-124_-21-123insACTAG
ENST00000624697.3:c.-21-124_-21-123insACTAG ENSP00000485643.1:n.-21-124_-21-123insACTAG
NM_005101.3:c.4-124_4-123insACTAG NP_005092.1:n.4-124_4-123insACTAG
NM_005101.4:c.4-124_4-123insACTAG MANE Select NP_005092.1:n.4-124_4-123insACTAG