Canonical Allele Identifier: CA1148845887
Gene: ISG15 HGNC NCBI

Linked Data

dbSNP Id: rs1644246997
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.1013965A>G , CM000663.2:g.1013965A>G GRCh38
NC_000001.10:g.949345A>G , CM000663.1:g.949345A>G GRCh37
NC_000001.9:g.939208A>G NCBI36
NG_033033.1:g.5499A>G
NG_033033.2:g.17828A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000624697.4:c.-21-19A>G ENSP00000485643.1:n.-21-19A>G
ENST00000649529.1:c.4-19A>G MANE Select ENSP00000496832.1:n.4-19A>G
ENST00000379389.4:c.4-19A>G ENSP00000368699.4:n.4-19A>G
ENST00000624652.1:c.-21-19A>G ENSP00000485313.1:n.-21-19A>G
ENST00000624697.3:c.-21-19A>G ENSP00000485643.1:n.-21-19A>G
NM_005101.3:c.4-19A>G NP_005092.1:n.4-19A>G
NM_005101.4:c.4-19A>G MANE Select NP_005092.1:n.4-19A>G
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