Canonical Allele Identifier: CA2642487238

Gene: ISG15

Linked Data

• gnomAD v4: 1-1013865-G-GC

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1013865_1013866insC , CM000663.2:g.1013865_1013866insC	GRCh38
NC_000001.10:g.949245_949246insC , CM000663.1:g.949245_949246insC	GRCh37
NC_000001.9:g.939108_939109insC	NCBI36
NG_033033.1:g.5399_5400insC
NG_033033.2:g.17728_17729insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000624697.4:c.-21-119_-21-118insC	ENSP00000485643.1:n.-21-119_-21-118insC
ENST00000649529.1:c.4-119_4-118insC MANE Select	ENSP00000496832.1:n.4-119_4-118insC
ENST00000379389.4:c.4-119_4-118insC	ENSP00000368699.4:n.4-119_4-118insC
ENST00000624652.1:c.-21-119_-21-118insC	ENSP00000485313.1:n.-21-119_-21-118insC
ENST00000624697.3:c.-21-119_-21-118insC	ENSP00000485643.1:n.-21-119_-21-118insC
NM_005101.3:c.4-119_4-118insC	NP_005092.1:n.4-119_4-118insC
NM_005101.4:c.4-119_4-118insC MANE Select	NP_005092.1:n.4-119_4-118insC