Canonical Allele Identifier: CA337804662

Gene: ISG15

Linked Data

• dbSNP Id: rs1644250096
• gnomAD v3: 1-1014237-T-C
• gnomAD v4: 1-1014237-T-C
• MyVariant Identifiers: chr1:g.949617T>C (hg19) ; chr1:g.1014237T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1014237T>C , CM000663.2:g.1014237T>C	GRCh38
NC_000001.10:g.949617T>C , CM000663.1:g.949617T>C	GRCh37
NC_000001.9:g.939480T>C	NCBI36
NG_033033.1:g.5771T>C
NG_033033.2:g.18100T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000624697.4:c.233T>C	ENSP00000485643.1:p.Val78Ala
ENST00000649529.1:c.257T>C MANE Select	ENSP00000496832.1:p.Val86Ala
ENST00000379389.4:c.257T>C	ENSP00000368699.4:p.Val86Ala
ENST00000624652.1:c.233T>C	ENSP00000485313.1:p.Val78Ala
ENST00000624697.3:c.233T>C	ENSP00000485643.1:p.Val78Ala
NM_005101.3:c.257T>C	NP_005092.1:p.Val86Ala
NM_005101.4:c.257T>C MANE Select	NP_005092.1:p.Val86Ala