Canonical Allele Identifier: CA415756727

Gene: ISG15

Linked Data

• MyVariant Identifiers: chr1:g.949552C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1014172C>T , CM000663.2:g.1014172C>T	GRCh38
NC_000001.10:g.949552C>T , CM000663.1:g.949552C>T	GRCh37
NC_000001.9:g.939415C>T	NCBI36
NG_033033.1:g.5706C>T
NG_033033.2:g.18035C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000624697.4:c.168C>T	ENSP00000485643.1:p.Gly56=
ENST00000649529.1:c.192C>T MANE Select	ENSP00000496832.1:p.Gly64=
ENST00000379389.4:c.192C>T	ENSP00000368699.4:p.Gly64=
ENST00000624652.1:c.168C>T	ENSP00000485313.1:p.Gly56=
ENST00000624697.3:c.168C>T	ENSP00000485643.1:p.Gly56=
NM_005101.3:c.192C>T	NP_005092.1:p.Gly64=
NM_005101.4:c.192C>T MANE Select	NP_005092.1:p.Gly64=