Canonical Allele Identifier: CA2642487286
Gene: ISG15 HGNC NCBI

Linked Data

gnomAD v4: 1-1013876-G-GT

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.1013876_1013877insT , CM000663.2:g.1013876_1013877insT GRCh38
NC_000001.10:g.949256_949257insT , CM000663.1:g.949256_949257insT GRCh37
NC_000001.9:g.939119_939120insT NCBI36
NG_033033.1:g.5410_5411insT
NG_033033.2:g.17739_17740insT

Transcript Alleles

HGVS Amino-acid Change
ENST00000624697.4:c.-21-108_-21-107insT ENSP00000485643.1:n.-21-108_-21-107insT
ENST00000649529.1:c.4-108_4-107insT MANE Select ENSP00000496832.1:n.4-108_4-107insT
ENST00000379389.4:c.4-108_4-107insT ENSP00000368699.4:n.4-108_4-107insT
ENST00000624652.1:c.-21-108_-21-107insT ENSP00000485313.1:n.-21-108_-21-107insT
ENST00000624697.3:c.-21-108_-21-107insT ENSP00000485643.1:n.-21-108_-21-107insT
NM_005101.3:c.4-108_4-107insT NP_005092.1:n.4-108_4-107insT
NM_005101.4:c.4-108_4-107insT MANE Select NP_005092.1:n.4-108_4-107insT