Canonical Allele Identifier: CA2742133449

Gene: ISG15

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1013866_1013867insT , CM000663.2:g.1013866_1013867insT	GRCh38
NC_000001.10:g.949246_949247insT , CM000663.1:g.949246_949247insT	GRCh37
NC_000001.9:g.939109_939110insT	NCBI36
NG_033033.1:g.5400_5401insT
NG_033033.2:g.17729_17730insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000624697.4:c.-21-118_-21-117insT	ENSP00000485643.1:n.-21-118_-21-117insT
ENST00000649529.1:c.4-118_4-117insT MANE Select	ENSP00000496832.1:n.4-118_4-117insT
ENST00000379389.4:c.4-118_4-117insT	ENSP00000368699.4:n.4-118_4-117insT
ENST00000624652.1:c.-21-118_-21-117insT	ENSP00000485313.1:n.-21-118_-21-117insT
ENST00000624697.3:c.-21-118_-21-117insT	ENSP00000485643.1:n.-21-118_-21-117insT
NM_005101.3:c.4-118_4-117insT	NP_005092.1:n.4-118_4-117insT
NM_005101.4:c.4-118_4-117insT MANE Select	NP_005092.1:n.4-118_4-117insT