Canonical Allele Identifier: CA2642487275
Gene: ISG15 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.1013873_1013874insTCT , CM000663.2:g.1013873_1013874insTCT GRCh38
NC_000001.10:g.949253_949254insTCT , CM000663.1:g.949253_949254insTCT GRCh37
NC_000001.9:g.939116_939117insTCT NCBI36
NG_033033.1:g.5407_5408insTCT
NG_033033.2:g.17736_17737insTCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000624697.4:c.-21-111_-21-110insTCT ENSP00000485643.1:n.-21-111_-21-110insTCT
ENST00000649529.1:c.4-111_4-110insTCT MANE Select ENSP00000496832.1:n.4-111_4-110insTCT
ENST00000379389.4:c.4-111_4-110insTCT ENSP00000368699.4:n.4-111_4-110insTCT
ENST00000624652.1:c.-21-111_-21-110insTCT ENSP00000485313.1:n.-21-111_-21-110insTCT
ENST00000624697.3:c.-21-111_-21-110insTCT ENSP00000485643.1:n.-21-111_-21-110insTCT
NM_005101.3:c.4-111_4-110insTCT NP_005092.1:n.4-111_4-110insTCT
NM_005101.4:c.4-111_4-110insTCT MANE Select NP_005092.1:n.4-111_4-110insTCT