Canonical Allele Identifier: CA2642487168

Gene: ISG15

Linked Data

• gnomAD v4: 1-1013858-G-GTT

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1013858_1013859insTT , CM000663.2:g.1013858_1013859insTT	GRCh38
NC_000001.10:g.949238_949239insTT , CM000663.1:g.949238_949239insTT	GRCh37
NC_000001.9:g.939101_939102insTT	NCBI36
NG_033033.1:g.5392_5393insTT
NG_033033.2:g.17721_17722insTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000624697.4:c.-21-126_-21-125insTT	ENSP00000485643.1:n.-21-126_-21-125insTT
ENST00000649529.1:c.4-126_4-125insTT MANE Select	ENSP00000496832.1:n.4-126_4-125insTT
ENST00000379389.4:c.4-126_4-125insTT	ENSP00000368699.4:n.4-126_4-125insTT
ENST00000624652.1:c.-21-126_-21-125insTT	ENSP00000485313.1:n.-21-126_-21-125insTT
ENST00000624697.3:c.-21-126_-21-125insTT	ENSP00000485643.1:n.-21-126_-21-125insTT
NM_005101.3:c.4-126_4-125insTT	NP_005092.1:n.4-126_4-125insTT
NM_005101.4:c.4-126_4-125insTT MANE Select	NP_005092.1:n.4-126_4-125insTT