Canonical Allele Identifier: CA337803463
Gene: ISG15 HGNC NCBI

Linked Data

gnomAD v4: 1-1014014-G-A
MyVariant Identifiers: chr1:g.949394G>A (hg19) chr1:g.1014014G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.1014014G>A , CM000663.2:g.1014014G>A GRCh38
NC_000001.10:g.949394G>A , CM000663.1:g.949394G>A GRCh37
NC_000001.9:g.939257G>A NCBI36
NG_033033.1:g.5548G>A
NG_033033.2:g.17877G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000624697.4:c.10G>A ENSP00000485643.1:p.Gly4Ser
ENST00000649529.1:c.34G>A MANE Select ENSP00000496832.1:p.Gly12Ser
ENST00000379389.4:c.34G>A ENSP00000368699.4:p.Gly12Ser
ENST00000624652.1:c.10G>A ENSP00000485313.1:p.Gly4Ser
ENST00000624697.3:c.10G>A ENSP00000485643.1:p.Gly4Ser
NM_005101.3:c.34G>A NP_005092.1:p.Gly12Ser
NM_005101.4:c.34G>A MANE Select NP_005092.1:p.Gly12Ser
Search 100 bp 5'
Search 100 bp 3'