Canonical Allele Identifier: CA2742133444
Gene: ISG15 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.1013859_1013860insTGTG , CM000663.2:g.1013859_1013860insTGTG GRCh38
NC_000001.10:g.949239_949240insTGTG , CM000663.1:g.949239_949240insTGTG GRCh37
NC_000001.9:g.939102_939103insTGTG NCBI36
NG_033033.1:g.5393_5394insTGTG
NG_033033.2:g.17722_17723insTGTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000624697.4:c.-21-125_-21-124insTGTG ENSP00000485643.1:n.-21-125_-21-124insTGTG
ENST00000649529.1:c.4-125_4-124insTGTG MANE Select ENSP00000496832.1:n.4-125_4-124insTGTG
ENST00000379389.4:c.4-125_4-124insTGTG ENSP00000368699.4:n.4-125_4-124insTGTG
ENST00000624652.1:c.-21-125_-21-124insTGTG ENSP00000485313.1:n.-21-125_-21-124insTGTG
ENST00000624697.3:c.-21-125_-21-124insTGTG ENSP00000485643.1:n.-21-125_-21-124insTGTG
NM_005101.3:c.4-125_4-124insTGTG NP_005092.1:n.4-125_4-124insTGTG
NM_005101.4:c.4-125_4-124insTGTG MANE Select NP_005092.1:n.4-125_4-124insTGTG