Canonical Allele Identifier: CA1148734765

Gene: ISG15

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1014233C= , CM000663.2:g.1014233C=	GRCh38
NC_000001.10:g.949613C= , CM000663.1:g.949613C=	GRCh37
NC_000001.9:g.939476C=	NCBI36
NG_033033.1:g.5767C=
NG_033033.2:g.18096C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000624697.4:c.229C=	ENSP00000485643.1:p.Leu77=
ENST00000649529.1:c.253C= MANE Select	ENSP00000496832.1:p.Leu85=
ENST00000379389.4:c.253C=	ENSP00000368699.4:p.Leu85=
ENST00000624652.1:c.229C=	ENSP00000485313.1:p.Leu77=
ENST00000624697.3:c.229C=	ENSP00000485643.1:p.Leu77=
NM_005101.3:c.253C=	NP_005092.1:p.Leu85=
NM_005101.4:c.253C= MANE Select	NP_005092.1:p.Leu85=