Canonical Allele Identifier: CA337803924

Gene: ISG15

Linked Data

• MyVariant Identifiers: chr1:g.949497C>T (hg19) ; chr1:g.1014117C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1014117C>T , CM000663.2:g.1014117C>T	GRCh38
NC_000001.10:g.949497C>T , CM000663.1:g.949497C>T	GRCh37
NC_000001.9:g.939360C>T	NCBI36
NG_033033.1:g.5651C>T
NG_033033.2:g.17980C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000624697.4:c.113C>T	ENSP00000485643.1:p.Ala38Val
ENST00000649529.1:c.137C>T MANE Select	ENSP00000496832.1:p.Ala46Val
ENST00000379389.4:c.137C>T	ENSP00000368699.4:p.Ala46Val
ENST00000624652.1:c.113C>T	ENSP00000485313.1:p.Ala38Val
ENST00000624697.3:c.113C>T	ENSP00000485643.1:p.Ala38Val
NM_005101.3:c.137C>T	NP_005092.1:p.Ala46Val
NM_005101.4:c.137C>T MANE Select	NP_005092.1:p.Ala46Val