Canonical Allele Identifier: CA1148845608

Gene: ISG15

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1013895G= , CM000663.2:g.1013895G=	GRCh38
NC_000001.10:g.949275G= , CM000663.1:g.949275G=	GRCh37
NC_000001.9:g.939138G=	NCBI36
NG_033033.1:g.5429G=
NG_033033.2:g.17758G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000624697.4:c.-21-89G=	ENSP00000485643.1:n.-21-89G=
ENST00000649529.1:c.4-89G= MANE Select	ENSP00000496832.1:n.4-89G=
ENST00000379389.4:c.4-89G=	ENSP00000368699.4:n.4-89G=
ENST00000624652.1:c.-21-89G=	ENSP00000485313.1:n.-21-89G=
ENST00000624697.3:c.-21-89G=	ENSP00000485643.1:n.-21-89G=
NM_005101.3:c.4-89G=	NP_005092.1:n.4-89G=
NM_005101.4:c.4-89G= MANE Select	NP_005092.1:n.4-89G=