Canonical Allele Identifier: CA337803513
Gene: ISG15 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.1014025C>G , CM000663.2:g.1014025C>G GRCh38
NC_000001.10:g.949405C>G , CM000663.1:g.949405C>G GRCh37
NC_000001.9:g.939268C>G NCBI36
NG_033033.1:g.5559C>G
NG_033033.2:g.17888C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000624697.4:c.21C>G ENSP00000485643.1:p.Phe7Leu
ENST00000649529.1:c.45C>G MANE Select ENSP00000496832.1:p.Phe15Leu
ENST00000379389.4:c.45C>G ENSP00000368699.4:p.Phe15Leu
ENST00000624652.1:c.21C>G ENSP00000485313.1:p.Phe7Leu
ENST00000624697.3:c.21C>G ENSP00000485643.1:p.Phe7Leu
NM_005101.3:c.45C>G NP_005092.1:p.Phe15Leu
NM_005101.4:c.45C>G MANE Select NP_005092.1:p.Phe15Leu