Canonical Allele Identifier: CA2642487221

Gene: ISG15

Linked Data

• gnomAD v4: 1-1013861-T-TCTCGGTGGTCGCC

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1013861_1013862insCTCGGTGGTCGCC , CM000663.2:g.1013861_1013862insCTCGGTGGTCGCC	GRCh38
NC_000001.10:g.949241_949242insCTCGGTGGTCGCC , CM000663.1:g.949241_949242insCTCGGTGGTCGCC	GRCh37
NC_000001.9:g.939104_939105insCTCGGTGGTCGCC	NCBI36
NG_033033.1:g.5395_5396insCTCGGTGGTCGCC
NG_033033.2:g.17724_17725insCTCGGTGGTCGCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000624697.4:c.-21-123_-21-122insCTCGGTGGTCGCC	ENSP00000485643.1:n.-21-123_-21-122insCTCGGTGGTCGCC
ENST00000649529.1:c.4-123_4-122insCTCGGTGGTCGCC MANE Select	ENSP00000496832.1:n.4-123_4-122insCTCGGTGGTCGCC
ENST00000379389.4:c.4-123_4-122insCTCGGTGGTCGCC	ENSP00000368699.4:n.4-123_4-122insCTCGGTGGTCGCC
ENST00000624652.1:c.-21-123_-21-122insCTCGGTGGTCGCC	ENSP00000485313.1:n.-21-123_-21-122insCTCGGTGGTCGCC
ENST00000624697.3:c.-21-123_-21-122insCTCGGTGGTCGCC	ENSP00000485643.1:n.-21-123_-21-122insCTCGGTGGTCGCC
NM_005101.3:c.4-123_4-122insCTCGGTGGTCGCC	NP_005092.1:n.4-123_4-122insCTCGGTGGTCGCC
NM_005101.4:c.4-123_4-122insCTCGGTGGTCGCC MANE Select	NP_005092.1:n.4-123_4-122insCTCGGTGGTCGCC