Canonical Allele Identifier: CA337804318

Gene: ISG15

Linked Data

• dbSNP Id: rs1644249550
• gnomAD v4: 1-1014183-G-A
• MyVariant Identifiers: chr1:g.949563G>A (hg19) ; chr1:g.1014183G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1014183G>A , CM000663.2:g.1014183G>A	GRCh38
NC_000001.10:g.949563G>A , CM000663.1:g.949563G>A	GRCh37
NC_000001.9:g.939426G>A	NCBI36
NG_033033.1:g.5717G>A
NG_033033.2:g.18046G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000624697.4:c.179G>A	ENSP00000485643.1:p.Gly60Asp
ENST00000649529.1:c.203G>A MANE Select	ENSP00000496832.1:p.Gly68Asp
ENST00000379389.4:c.203G>A	ENSP00000368699.4:p.Gly68Asp
ENST00000624652.1:c.179G>A	ENSP00000485313.1:p.Gly60Asp
ENST00000624697.3:c.179G>A	ENSP00000485643.1:p.Gly60Asp
NM_005101.3:c.203G>A	NP_005092.1:p.Gly68Asp
NM_005101.4:c.203G>A MANE Select	NP_005092.1:p.Gly68Asp