Canonical Allele Identifier: CA2642487100

Gene: ISG15

Linked Data

• gnomAD v4: 1-1013832-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1013832T>A , CM000663.2:g.1013832T>A	GRCh38
NC_000001.10:g.949212T>A , CM000663.1:g.949212T>A	GRCh37
NC_000001.9:g.939075T>A	NCBI36
NG_033033.1:g.5366T>A
NG_033033.2:g.17695T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000624697.4:c.-21-152T>A	ENSP00000485643.1:n.-21-152T>A
ENST00000649529.1:c.4-152T>A MANE Select	ENSP00000496832.1:n.4-152T>A
ENST00000379389.4:c.4-152T>A	ENSP00000368699.4:n.4-152T>A
ENST00000624652.1:c.-21-152T>A	ENSP00000485313.1:n.-21-152T>A
ENST00000624697.3:c.-21-152T>A	ENSP00000485643.1:n.-21-152T>A
NM_005101.3:c.4-152T>A	NP_005092.1:n.4-152T>A
NM_005101.4:c.4-152T>A MANE Select	NP_005092.1:n.4-152T>A