Canonical Allele Identifier: CA415756215

Gene: ISG15

Linked Data

• ClinVar Variation Id: 1610388
• ClinVar RCV Id: RCV002145229
• dbSNP Id: rs367963389
• MyVariant Identifiers: chr1:g.949450G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1014070G>T , CM000663.2:g.1014070G>T	GRCh38
NC_000001.10:g.949450G>T , CM000663.1:g.949450G>T	GRCh37
NC_000001.9:g.939313G>T	NCBI36
NG_033033.1:g.5604G>T
NG_033033.2:g.17933G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000624697.4:c.66G>T	ENSP00000485643.1:p.Ala22=
ENST00000649529.1:c.90G>T MANE Select	ENSP00000496832.1:p.Ala30=
ENST00000379389.4:c.90G>T	ENSP00000368699.4:p.Ala30=
ENST00000624652.1:c.66G>T	ENSP00000485313.1:p.Ala22=
ENST00000624697.3:c.66G>T	ENSP00000485643.1:p.Ala22=
NM_005101.3:c.90G>T	NP_005092.1:p.Ala30=
NM_005101.4:c.90G>T MANE Select	NP_005092.1:p.Ala30=