Canonical Allele Identifier: CA16724830

Gene: ISG15

Linked Data

• dbSNP Id: rs939929604
• gnomAD v3: 1-1013854-G-A
• gnomAD v4: 1-1013854-G-A
• MyVariant Identifiers: chr1:g.949234G>A (hg19) ; chr1:g.1013854G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1013854G>A , CM000663.2:g.1013854G>A	GRCh38
NC_000001.10:g.949234G>A , CM000663.1:g.949234G>A	GRCh37
NC_000001.9:g.939097G>A	NCBI36
NG_033033.1:g.5388G>A
NG_033033.2:g.17717G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000624697.4:c.-21-130G>A	ENSP00000485643.1:n.-21-130G>A
ENST00000649529.1:c.4-130G>A MANE Select	ENSP00000496832.1:n.4-130G>A
ENST00000379389.4:c.4-130G>A	ENSP00000368699.4:n.4-130G>A
ENST00000624652.1:c.-21-130G>A	ENSP00000485313.1:n.-21-130G>A
ENST00000624697.3:c.-21-130G>A	ENSP00000485643.1:n.-21-130G>A
NM_005101.3:c.4-130G>A	NP_005092.1:n.4-130G>A
NM_005101.4:c.4-130G>A MANE Select	NP_005092.1:n.4-130G>A