Canonical Allele Identifier: CA2642487222

Gene: ISG15

Linked Data

• gnomAD v4: 1-1013861-T-TA

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1013861_1013862insA , CM000663.2:g.1013861_1013862insA	GRCh38
NC_000001.10:g.949241_949242insA , CM000663.1:g.949241_949242insA	GRCh37
NC_000001.9:g.939104_939105insA	NCBI36
NG_033033.1:g.5395_5396insA
NG_033033.2:g.17724_17725insA

Transcript Alleles

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