Canonical Allele Identifier: CA337803498

Gene: ISG15

Linked Data

• MyVariant Identifiers: chr1:g.949402A>C (hg19) ; chr1:g.1014022A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1014022A>C , CM000663.2:g.1014022A>C	GRCh38
NC_000001.10:g.949402A>C , CM000663.1:g.949402A>C	GRCh37
NC_000001.9:g.939265A>C	NCBI36
NG_033033.1:g.5556A>C
NG_033033.2:g.17885A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000624697.4:c.18A>C	ENSP00000485643.1:p.Glu6Asp
ENST00000649529.1:c.42A>C MANE Select	ENSP00000496832.1:p.Glu14Asp
ENST00000379389.4:c.42A>C	ENSP00000368699.4:p.Glu14Asp
ENST00000624652.1:c.18A>C	ENSP00000485313.1:p.Glu6Asp
ENST00000624697.3:c.18A>C	ENSP00000485643.1:p.Glu6Asp
NM_005101.3:c.42A>C	NP_005092.1:p.Glu14Asp
NM_005101.4:c.42A>C MANE Select	NP_005092.1:p.Glu14Asp