Canonical Allele Identifier: CA2642487283
Gene: ISG15 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.1013875_1013876insTCTC , CM000663.2:g.1013875_1013876insTCTC GRCh38
NC_000001.10:g.949255_949256insTCTC , CM000663.1:g.949255_949256insTCTC GRCh37
NC_000001.9:g.939118_939119insTCTC NCBI36
NG_033033.1:g.5409_5410insTCTC
NG_033033.2:g.17738_17739insTCTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000624697.4:c.-21-109_-21-108insTCTC ENSP00000485643.1:n.-21-109_-21-108insTCTC
ENST00000649529.1:c.4-109_4-108insTCTC MANE Select ENSP00000496832.1:n.4-109_4-108insTCTC
ENST00000379389.4:c.4-109_4-108insTCTC ENSP00000368699.4:n.4-109_4-108insTCTC
ENST00000624652.1:c.-21-109_-21-108insTCTC ENSP00000485313.1:n.-21-109_-21-108insTCTC
ENST00000624697.3:c.-21-109_-21-108insTCTC ENSP00000485643.1:n.-21-109_-21-108insTCTC
NM_005101.3:c.4-109_4-108insTCTC NP_005092.1:n.4-109_4-108insTCTC
NM_005101.4:c.4-109_4-108insTCTC MANE Select NP_005092.1:n.4-109_4-108insTCTC