Canonical Allele Identifier: CA415756339

Gene: ISG15

Linked Data

• MyVariant Identifiers: chr1:g.949492T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1014112T>A , CM000663.2:g.1014112T>A	GRCh38
NC_000001.10:g.949492T>A , CM000663.1:g.949492T>A	GRCh37
NC_000001.9:g.939355T>A	NCBI36
NG_033033.1:g.5646T>A
NG_033033.2:g.17975T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000624697.4:c.108T>A	ENSP00000485643.1:p.Arg36=
ENST00000649529.1:c.132T>A MANE Select	ENSP00000496832.1:p.Arg44=
ENST00000379389.4:c.132T>A	ENSP00000368699.4:p.Arg44=
ENST00000624652.1:c.108T>A	ENSP00000485313.1:p.Arg36=
ENST00000624697.3:c.108T>A	ENSP00000485643.1:p.Arg36=
NM_005101.3:c.132T>A	NP_005092.1:p.Arg44=
NM_005101.4:c.132T>A MANE Select	NP_005092.1:p.Arg44=