Canonical Allele Identifier: CA1144769522

Gene: ISG15

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1014268C= , CM000663.2:g.1014268C=	GRCh38
NC_000001.10:g.949648C= , CM000663.1:g.949648C=	GRCh37
NC_000001.9:g.939511C=	NCBI36
NG_033033.1:g.5802C=
NG_033033.2:g.18131C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000624697.4:c.264C=	ENSP00000485643.1:p.Tyr88=
ENST00000649529.1:c.288C= MANE Select	ENSP00000496832.1:p.Tyr96=
ENST00000379389.4:c.288C=	ENSP00000368699.4:p.Tyr96=
ENST00000624652.1:c.264C=	ENSP00000485313.1:p.Tyr88=
ENST00000624697.3:c.264C=	ENSP00000485643.1:p.Tyr88=
NM_005101.3:c.288C=	NP_005092.1:p.Tyr96=
NM_005101.4:c.288C= MANE Select	NP_005092.1:p.Tyr96=