Canonical Allele Identifier: CA2642487262

Gene: ISG15

Linked Data

• gnomAD v4: 1-1013870-C-CTGTGT

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1013870_1013871insTGTGT , CM000663.2:g.1013870_1013871insTGTGT	GRCh38
NC_000001.10:g.949250_949251insTGTGT , CM000663.1:g.949250_949251insTGTGT	GRCh37
NC_000001.9:g.939113_939114insTGTGT	NCBI36
NG_033033.1:g.5404_5405insTGTGT
NG_033033.2:g.17733_17734insTGTGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000624697.4:c.-21-114_-21-113insTGTGT	ENSP00000485643.1:n.-21-114_-21-113insTGTGT
ENST00000649529.1:c.4-114_4-113insTGTGT MANE Select	ENSP00000496832.1:n.4-114_4-113insTGTGT
ENST00000379389.4:c.4-114_4-113insTGTGT	ENSP00000368699.4:n.4-114_4-113insTGTGT
ENST00000624652.1:c.-21-114_-21-113insTGTGT	ENSP00000485313.1:n.-21-114_-21-113insTGTGT
ENST00000624697.3:c.-21-114_-21-113insTGTGT	ENSP00000485643.1:n.-21-114_-21-113insTGTGT
NM_005101.3:c.4-114_4-113insTGTGT	NP_005092.1:n.4-114_4-113insTGTGT
NM_005101.4:c.4-114_4-113insTGTGT MANE Select	NP_005092.1:n.4-114_4-113insTGTGT