Canonical Allele Identifier: CA337804959

Gene: ISG15

Linked Data

• gnomAD v4: 1-1014288-C-T
• MyVariant Identifiers: chr1:g.949668C>T (hg19) ; chr1:g.1014288C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1014288C>T , CM000663.2:g.1014288C>T	GRCh38
NC_000001.10:g.949668C>T , CM000663.1:g.949668C>T	GRCh37
NC_000001.9:g.939531C>T	NCBI36
NG_033033.1:g.5822C>T
NG_033033.2:g.18151C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000624697.4:c.284C>T	ENSP00000485643.1:p.Thr95Ile
ENST00000649529.1:c.308C>T MANE Select	ENSP00000496832.1:p.Thr103Ile
ENST00000379389.4:c.308C>T	ENSP00000368699.4:p.Thr103Ile
ENST00000624652.1:c.284C>T	ENSP00000485313.1:p.Thr95Ile
ENST00000624697.3:c.284C>T	ENSP00000485643.1:p.Thr95Ile
NM_005101.3:c.308C>T	NP_005092.1:p.Thr103Ile
NM_005101.4:c.308C>T MANE Select	NP_005092.1:p.Thr103Ile