Canonical Allele Identifier: CA2642487336

Gene: ISG15

Linked Data

• gnomAD v4: 1-1013898-A-AT

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1013898_1013899insT , CM000663.2:g.1013898_1013899insT	GRCh38
NC_000001.10:g.949278_949279insT , CM000663.1:g.949278_949279insT	GRCh37
NC_000001.9:g.939141_939142insT	NCBI36
NG_033033.1:g.5432_5433insT
NG_033033.2:g.17761_17762insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000624697.4:c.-21-86_-21-85insT	ENSP00000485643.1:n.-21-86_-21-85insT
ENST00000649529.1:c.4-86_4-85insT MANE Select	ENSP00000496832.1:n.4-86_4-85insT
ENST00000379389.4:c.4-86_4-85insT	ENSP00000368699.4:n.4-86_4-85insT
ENST00000624652.1:c.-21-86_-21-85insT	ENSP00000485313.1:n.-21-86_-21-85insT
ENST00000624697.3:c.-21-86_-21-85insT	ENSP00000485643.1:n.-21-86_-21-85insT
NM_005101.3:c.4-86_4-85insT	NP_005092.1:n.4-86_4-85insT
NM_005101.4:c.4-86_4-85insT MANE Select	NP_005092.1:n.4-86_4-85insT