Canonical Allele Identifier: CA1148734116

Gene: ISG15

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1014091C= , CM000663.2:g.1014091C=	GRCh38
NC_000001.10:g.949471C= , CM000663.1:g.949471C=	GRCh37
NC_000001.9:g.939334C=	NCBI36
NG_033033.1:g.5625C=
NG_033033.2:g.17954C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000624697.4:c.87C=	ENSP00000485643.1:p.Gly29=
ENST00000649529.1:c.111C= MANE Select	ENSP00000496832.1:p.Gly37=
ENST00000379389.4:c.111C=	ENSP00000368699.4:p.Gly37=
ENST00000624652.1:c.87C=	ENSP00000485313.1:p.Gly29=
ENST00000624697.3:c.87C=	ENSP00000485643.1:p.Gly29=
NM_005101.3:c.111C=	NP_005092.1:p.Gly37=
NM_005101.4:c.111C= MANE Select	NP_005092.1:p.Gly37=