Canonical Allele Identifier: CA2642487319
Gene: ISG15 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.1013886_1013887insCCAGGGACAGTGCTCCCTCCTGTC , CM000663.2:g.1013886_1013887insCCAGGGACAGTGCTCCCTCCTGTC GRCh38
NC_000001.10:g.949266_949267insCCAGGGACAGTGCTCCCTCCTGTC , CM000663.1:g.949266_949267insCCAGGGACAGTGCTCCCTCCTGTC GRCh37
NC_000001.9:g.939129_939130insCCAGGGACAGTGCTCCCTCCTGTC NCBI36
NG_033033.1:g.5420_5421insCCAGGGACAGTGCTCCCTCCTGTC
NG_033033.2:g.17749_17750insCCAGGGACAGTGCTCCCTCCTGTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000624697.4:c.-21-98_-21-97insCCAGGGACAGTGCTCCCTCCTGTC ENSP00000485643.1:n.-21-98_-21-97insCCAGGGACAGTGCTCCCTCCTGTC
ENST00000649529.1:c.4-98_4-97insCCAGGGACAGTGCTCCCTCCTGTC MANE Select ENSP00000496832.1:n.4-98_4-97insCCAGGGACAGTGCTCCCTCCTGTC
ENST00000379389.4:c.4-98_4-97insCCAGGGACAGTGCTCCCTCCTGTC ENSP00000368699.4:n.4-98_4-97insCCAGGGACAGTGCTCCCTCCTGTC
ENST00000624652.1:c.-21-98_-21-97insCCAGGGACAGTGCTCCCTCCTGTC ENSP00000485313.1:n.-21-98_-21-97insCCAGGGACAGTGCTCCCTCCTGTC
ENST00000624697.3:c.-21-98_-21-97insCCAGGGACAGTGCTCCCTCCTGTC ENSP00000485643.1:n.-21-98_-21-97insCCAGGGACAGTGCTCCCTCCTGTC
NM_005101.3:c.4-98_4-97insCCAGGGACAGTGCTCCCTCCTGTC NP_005092.1:n.4-98_4-97insCCAGGGACAGTGCTCCCTCCTGTC
NM_005101.4:c.4-98_4-97insCCAGGGACAGTGCTCCCTCCTGTC MANE Select NP_005092.1:n.4-98_4-97insCCAGGGACAGTGCTCCCTCCTGTC