Canonical Allele Identifier: CA520625479

Gene: ISG15

Linked Data

• dbSNP Id: rs1557674264
• gnomAD v2: 1-949614-TG-T
• gnomAD v4: 1-1014234-TG-T
• MyVariant Identifiers: chr1:g.949615del (hg19) ; chr1:g.1014235del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1014236del , CM000663.2:g.1014236del	GRCh38
NC_000001.10:g.949616del , CM000663.1:g.949616del	GRCh37
NC_000001.9:g.939479del	NCBI36
NG_033033.1:g.5770del
NG_033033.2:g.18099del

Transcript Alleles

HGVS	Amino-acid change
ENST00000624697.4:c.232del	ENSP00000485643.1:p.Val78Ter
ENST00000649529.1:c.256del MANE Select	ENSP00000496832.1:p.Val86Ter
ENST00000379389.4:c.256del	ENSP00000368699.4:p.Val86Ter
ENST00000624652.1:c.232del	ENSP00000485313.1:p.Val78Ter
ENST00000624697.3:c.232del	ENSP00000485643.1:p.Val78Ter
NM_005101.3:c.256del	NP_005092.1:p.Val86Ter
NM_005101.4:c.256del MANE Select	NP_005092.1:p.Val86Ter