Canonical Allele Identifier: CA997657685
Gene: ISG15 HGNC NCBI

Linked Data

dbSNP Id: rs1644248807
gnomAD v3: 1-1014139-G-GC
gnomAD v4: 1-1014139-G-GC

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.1014140dup , CM000663.2:g.1014140dup GRCh38
NC_000001.10:g.949520dup , CM000663.1:g.949520dup GRCh37
NC_000001.9:g.939383dup NCBI36
NG_033033.1:g.5674dup
NG_033033.2:g.18003dup

Transcript Alleles

HGVS Amino-acid change
ENST00000624697.4:c.136dup ENSP00000485643.1:p.Leu46ProfsTer?
ENST00000649529.1:c.160dup MANE Select ENSP00000496832.1:p.Leu54ProfsTer?
ENST00000379389.4:c.160dup ENSP00000368699.4:p.Leu54ProfsTer?
ENST00000624652.1:c.136dup ENSP00000485313.1:p.Leu46ProfsTer?
ENST00000624697.3:c.136dup ENSP00000485643.1:p.Leu46ProfsTer?
NM_005101.3:c.160dup NP_005092.1:p.Leu54ProfsTer?
NM_005101.4:c.160dup MANE Select NP_005092.1:p.Leu54ProfsTer?