Canonical Allele Identifier: CA1141684773

Gene: ISG15

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1014131G= , CM000663.2:g.1014131G=	GRCh38
NC_000001.10:g.949511G= , CM000663.1:g.949511G=	GRCh37
NC_000001.9:g.939374G=	NCBI36
NG_033033.1:g.5665G=
NG_033033.2:g.17994G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000624697.4:c.127G=	ENSP00000485643.1:p.Gly43=
ENST00000649529.1:c.151G= MANE Select	ENSP00000496832.1:p.Gly51=
ENST00000379389.4:c.151G=	ENSP00000368699.4:p.Gly51=
ENST00000624652.1:c.127G=	ENSP00000485313.1:p.Gly43=
ENST00000624697.3:c.127G=	ENSP00000485643.1:p.Gly43=
NM_005101.3:c.151G=	NP_005092.1:p.Gly51=
NM_005101.4:c.151G= MANE Select	NP_005092.1:p.Gly51=