Canonical Allele Identifier: CA337803812

Gene: ISG15

Linked Data

• gnomAD v4: 1-1014097-C-A
• MyVariant Identifiers: chr1:g.949477C>A (hg19) ; chr1:g.1014097C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1014097C>A , CM000663.2:g.1014097C>A	GRCh38
NC_000001.10:g.949477C>A , CM000663.1:g.949477C>A	GRCh37
NC_000001.9:g.939340C>A	NCBI36
NG_033033.1:g.5631C>A
NG_033033.2:g.17960C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000624697.4:c.93C>A	ENSP00000485643.1:p.His31Gln
ENST00000649529.1:c.117C>A MANE Select	ENSP00000496832.1:p.His39Gln
ENST00000379389.4:c.117C>A	ENSP00000368699.4:p.His39Gln
ENST00000624652.1:c.93C>A	ENSP00000485313.1:p.His31Gln
ENST00000624697.3:c.93C>A	ENSP00000485643.1:p.His31Gln
NM_005101.3:c.117C>A	NP_005092.1:p.His39Gln
NM_005101.4:c.117C>A MANE Select	NP_005092.1:p.His39Gln