Canonical Allele Identifier: CA337803646

Gene: ISG15

Linked Data

• dbSNP Id: rs1392952648
• gnomAD v2: 1-949442-C-A
• gnomAD v4: 1-1014062-C-A
• MyVariant Identifiers: chr1:g.949442C>A (hg19) ; chr1:g.1014062C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1014062C>A , CM000663.2:g.1014062C>A	GRCh38
NC_000001.10:g.949442C>A , CM000663.1:g.949442C>A	GRCh37
NC_000001.9:g.939305C>A	NCBI36
NG_033033.1:g.5596C>A
NG_033033.2:g.17925C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000624697.4:c.58C>A	ENSP00000485643.1:p.Leu20Met
ENST00000649529.1:c.82C>A MANE Select	ENSP00000496832.1:p.Leu28Met
ENST00000379389.4:c.82C>A	ENSP00000368699.4:p.Leu28Met
ENST00000624652.1:c.58C>A	ENSP00000485313.1:p.Leu20Met
ENST00000624697.3:c.58C>A	ENSP00000485643.1:p.Leu20Met
NM_005101.3:c.82C>A	NP_005092.1:p.Leu28Met
NM_005101.4:c.82C>A MANE Select	NP_005092.1:p.Leu28Met