Canonical Allele Identifier: CA2742133454
Gene: ISG15 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.1013869_1013870insT , CM000663.2:g.1013869_1013870insT GRCh38
NC_000001.10:g.949249_949250insT , CM000663.1:g.949249_949250insT GRCh37
NC_000001.9:g.939112_939113insT NCBI36
NG_033033.1:g.5403_5404insT
NG_033033.2:g.17732_17733insT

Transcript Alleles

HGVS Amino-acid Change
ENST00000624697.4:c.-21-115_-21-114insT ENSP00000485643.1:n.-21-115_-21-114insT
ENST00000649529.1:c.4-115_4-114insT MANE Select ENSP00000496832.1:n.4-115_4-114insT
ENST00000379389.4:c.4-115_4-114insT ENSP00000368699.4:n.4-115_4-114insT
ENST00000624652.1:c.-21-115_-21-114insT ENSP00000485313.1:n.-21-115_-21-114insT
ENST00000624697.3:c.-21-115_-21-114insT ENSP00000485643.1:n.-21-115_-21-114insT
NM_005101.3:c.4-115_4-114insT NP_005092.1:n.4-115_4-114insT
NM_005101.4:c.4-115_4-114insT MANE Select NP_005092.1:n.4-115_4-114insT